Skip to content

Developing a Positive Psychology Intervention to Promote Health Behaviors in Metabolic Syndrome: Proof-of Concept Trial

Developing a Positive Psychology Intervention to Promote Health Behaviors in Metabolic Syndrome: Proof-of Concept Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03473886
Acronym
MAPP-II
Enrollment
8
Registered
2018-03-22
Start date
2018-06-01
Completion date
2019-06-01
Last updated
2020-05-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Metabolic Syndrome

Brief summary

Specific Aim #1 (Feasibility; primary aim): To assess the feasibility of the positive psychology (PP)-motivational interviewing (MI) group-based physical activity intervention and outcome assessments in patients with metabolic syndrome (MetS). Hypothesis: The PP exercises and MI-based goal-setting sessions will be feasible: most (≥50%) of participants will complete 6/8 exercises/sessions. Furthermore, we will be able to obtain objective physical activity measurement follow-up data from at least 80% of enrolled participants at 8 weeks. Specific Aim #2 (Acceptability): To assess whether the intervention is acceptable to participants, as measured by ratings provided after each PP and MI exercise. Hypothesis: The intervention will be acceptable: participants will rate each PP and MI exercise with a mean score of at least 7 out of 10 on ratings of ease of completion and helpfulness. Specific Aim #3 (Outcomes): To assess whether this preliminary intervention appears to result in improvement of physical activity, related health behaviors (sedentary time, diet quality), and psychological well-being (optimism, positive affect, anxiety, depression). Hypothesis: The intervention will lead to improvements in physical activity, related health behaviors, optimism and positive affect, and reductions in depression and anxiety at 8 weeks compared to baseline.

Detailed description

In this proof-of-concept study, investigators will run two 8-week PP-MI groups (complete n=8 each, n=16 total) for primary care patients with MetS. Investigators will use ratings of feasibility and acceptability for each of the sessions and obtain objective physical activity measures pre- and post- group. Investigators will also obtain questionnaire-based information related to health behavior adherence and psychological and physical health to ensure the feasibility of these methods prior to further testing. Investigators may gather exit interview data to assess participant liking, utility, and additional needs, to allow for further refinement of the intervention. Baseline information about enrolled participants will be obtained from the patients, care providers, and the electronic medical record as required for characterization of the population. This information will include medical data related to MetS (e.g., blood sugar, blood pressure, body mass index, triglycerides, cholesterol), current medications, and sociodemographic data (age, gender, race/ethnicity, education, marital status). Participants will attend 90-minute groups sessions that will be held at two primary care clinics (MGH Healthcare Centers). The overall structure of each session will be: 30 minutes for positive psychology exercise review/discussion, 30 minutes for physical activity goal setting, education, and discussion, and 30 minutes for a group walk or indoor exercises in inclement weather. Participants will be asked to wear an Actigraph GT3x+ accelerometer for 1 week at baseline and 1 week at follow-up to assess the feasibility of doing so. Accelerometers such as this one are considered to be the standard for measuring habitual physical activity. They are pedometer-size devices that attach to a belt and are worn at the waist. Participants will also be given a Fitbit Zip to keep, which they will be asked to wear daily for the duration of the study in order to track their activity (steps). Upon beginning the groups, participants will be provided with a treatment manual with weekly PP exercises, information about the importance of physical activity and related health behaviors, and how to set goals to improve these behaviors. The PI will lead all groups. For the first session, in the PP portion, participants will discuss and be assigned the first exercise- gratitude for positive events- and will be instructed to complete the PP exercise during the next week. Prior to completing the exercise, participants will be asked to rate their current levels of happiness and optimism. Immediately after completing the exercise, participants will rate the ease of exercise completion, overall utility of the exercise, and their current levels of happiness and optimism, all using 10-point Likert scales. In the first goal-setting session, we will discuss the importance of physical activity in MetS. Participants will be given a Fitbit Zip to keep, which they will use to track the number of steps they take each day, for the duration of the study. Investigators will review instructions for use and set a goal for monitoring their baseline physical activity over the next week. Fitbits will not be used as an outcome measure but as a tool that participants can use to monitor their activity and set goals. Finally, the last 30 minutes will be spent doing a group walk around the local clinic neighborhood. All group walks and exercises will be done at a pace comfortable for participants. Participants will be asked to complete the 8 total weekly PP exercises, set physical activity goals, and attend as many group sessions as they can. All sessions will include (a) a review and discussion of the past week's PP exercise, (b) a discussion of the rationale of the next week's PP exercise using the PP manual, and (c) assignment of the next week's PP exercise. For the goal-setting/MI portion, participants will (a) review their goals and steps from the prior week, (b) discuss techniques for improving physical activity (e.g., monitoring physical activity, taking standing breaks), and (c) set goals for the next week. The exercises and content for both PP and MI will be assigned in the same order for all participants receiving them. Immediately after the week 8 session, investigators will distribute the same self-report questionnaires that were administered at baseline (before week 1). The Actigraphs will then be collected at this point and the data will be uploaded to assess for valid wear time. If participants have not worn them for enough time (\>4 days), investigators will send it home with them and ask them to re-wear it and mail it back.

Interventions

BEHAVIORALIntervention arm: PP-MI

The positive psychology exercises include gratitude-based activities, strengths-based activities, and meaning-based activities. The physical activity goal setting exercises include the following topics: health benefits, social resources, and neighborhood walkability.

Sponsors

Massachusetts General Hospital
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 100 Years
Healthy volunteers
No

Inclusion criteria

• Both of the two MetS components most strongly related to MetS outcomes and most sensitive to lifestyle change: * elevated abdominal obesity (waist circumference \>102 cm in men or \>88 cm in women) * If waist circumference is not available, body mass index (BMI) will be used as a surrogate measure based on prior research (BMI ≥29.1 kg/m2 for men and 27.2 kg/m2 for women). AND \- elevated blood pressure (systolic ≥130 and/or diastolic ≥85 mm Hg or be on blood pressure medication). * Plus ≥1 additional MetS component: * Serum triglycerides ≥150 mg/dL * High-density lipoprotein (HDL) cholesterol \<40 mg/dL in men or \<50 mg/dL in women * Fasting plasma glucose \>100mg/dL. * Suboptimal physical activity defined as ≤150 minutes/week moderate intensity activity, which represents less than national-level recommendations.

Exclusion criteria

* Inability to speak/read English * Cognitive deficits impeding ability to participate or provide informed consent (measured by a 6-item screen) * Illness likely to lead to death in the next 6 months per PCP * Current treatment for cancer, liver, or renal disease * Pregnancy * Documented severe mental illness (e.g., psychosis, suicidality) * No telephone access * Inability to be physically active * Diabetes or known or suggested cardiac disease, given that this is a primary prevention study.

Design outcomes

Primary

MeasureTime frameDescription
Number of PP-MI-Based Health Behavior Intervention Exercises Completed8 weeks of group sessionsFeasibility will be measured by examining the number of completed exercises.
Number of Participants Completing Objective Physical Activity Measurement8 weeks of group sessionsFeasibility will be measured by examining the number of participants who wore Actigraphs with sufficient wear time both at baseline and at follow-up

Secondary

MeasureTime frameDescription
Changes in Life Orientation Test- Revised ScoresChange in dispositional optimism from baseline to 8 weeksLife Orientation Test-Revised (LOT-R) is a well-validated 6-item instrument used to measure dispositional optimism. (Range: 0-24) Change was calculated by subtracting the score at baseline from the score at 8 weeks. Higher scores indicate higher levels of optimism.
Changes in Positive and Negative Affect Schedule ScoresChange in score from Baseline to 8 weeksThe positive affect items on the Positive and Negative Affect Schedule (PANAS), a well-validated scale used in other intervention trials and in patients with HF, will be used to measure positive affect. (Range: 10-50). Change was calculated by subtracting the score at baseline from the score at 8 weeks. Higher scores indicate higher levels of positive affect.
Changes in The HADS-A ScoresChange in score from Baseline to 8 weeksThe Hospital Anxiety and Depression Scale will be used to measure depression and anxiety. This is a well-validated scale with few somatic symptom items that can confound mood/anxiety assessment in medically-ill patients. (Range:0-21) Change was calculated by subtracting the score at baseline from the score at 8 weeks. Higher scores indicate higher levels of anxiety.
Changes in The Neighborhood Environment Walkability Scale-Abbreviated ScoresChange in score from Baseline to 8 weeksMeasure Description: NEWS is a 98-question instrument that assesses the perception of neighborhood design features related to physical activity. NEWS-A is an abbreviated version and will be used to measure residents' perceptions of neighborhood design related to physical activity, including places for walking and cycling, aesthetics, traffic hazards, and crime (Range: 16-64). Higher scores indicate greater perceived walkability.
Changes in Barriers to Being Active Quiz- Lack of Time ScoresBaseline and 8 weeksThe BBAQ is a 21-item measure, published by the US Centers for Disease Control and Prevention (CDC), assessing the following barriers to physical activity: 1) lack of time, 2) social influence, 3) lack of energy, 4) lack of willpower, 5) fear of injury, 6) lack of skill, and 7) lack of resources (eg, recreational facilities, exercise equipment). Each domain contains 3 items, with a total score range of 0 to 63. Respondents rate the degree of activity interference on a 4-point scale, ranging from 0 = very unlikely to 3 = very likely. This outcome explores lack of time category (range of 0-9), and we calculated the change in score from baseline to 8 weeks.
Changes in The Medical Outcomes Study Short Form-12 Scores - Physical Composite ScoreChange in score from Baseline to 8 weeksThe Medical Outcomes Study Short Form-12 (SF-12) will be used to measure quality of life. This is an instrument which has been used in multiple cardiac studies in the past. (SF-12 Mental Composite Score and Physical Composite Score Range: 0-100 each). Change was calculated by subtracting the score at baseline from the score at 8 weeks. Higher scores indicate higher level of health related QoL.
Changes in The Community Healthy Activities Model Program for Seniors ScoresChange in score from Baseline to 8 weeksCHAMP is a self-report questionnaire that assesses weekly frequency and duration of a variety of lifestyle physical activities that are meaningful and appropriate for older adults. It includes activities of various intensities (from light to vigorous) such as walking, running, hiking, swimming, bicycling, dancing, tennis, aerobics, yoga/tai chi, gardening, and housework. The activities are assessed in min/week.
Changes in Behavioral Risk Factor Surveillance System Fruit and Vegetable Module - Fruit CategoryChange in # of fruits consumed/day from Baseline to 8 weeksMeasure Description: The CDC's BRFSS Fruit and Vegetable Module is a brief questionnaire about frequency of eating different types of fruits and vegetables. It assesses the frequency of consumption of 100% fruit juice, fruit, beans (legumes), dark green vegetables, orange vegetables, and other vegetables over the past month. The outcome measure is the number of fruits consumed per day.
Changes in National Cancer Institute's Percentage Energy From Fat Screener ScoresChange in number of times fat is consumed per day from Baseline to 8 weeksThe National Cancer Institute's Percentage Energy from Fat Screen is a brief questionnaire that estimates people's typical percentage of energy derived from eating common fat-containing foods, as fat content is related to metabolic syndrome progression. The questionnaire converts an individual's responses to an estimate of that individual's percentage energy from fat. Higher scores indicate higher fat consumption.
Acceptability of Intervention8 weeksAcceptability of the intervention was assessed through participants' ratings of each PP and MI exercise. Participants will provide ratings of utility after each exercise, measured on a 10-point Likert scale (0=not at all helpful;10=very helpful). Weekly utility ratings were averaged to provide an overall utility score of the exercises.
Change in Barriers to Being Active Quiz Score- Social InfluenceChange in score from Baseline to 8 weeksThe BBAQ is a 21-item measure, published by the US Centers for Disease Control and Prevention (CDC), assessing the following barriers to physical activity: 1) lack of time, 2) social influence, 3) lack of energy, 4) lack of willpower, 5) fear of injury, 6) lack of skill, and 7) lack of resources (eg, recreational facilities, exercise equipment). Each domain contains 3 items, with a total score range of 0 to 63. Respondents rate the degree of activity interference on a 4-point scale, ranging from 0 = very unlikely to 3 = very likely. This outcome explores social influence category (range of 0-9), and we calculated the change in score from baseline to 8 weeks.
Change in Barriers to Being Active Quiz Score- Lack of EnergyChange in score from Baseline to 8 weeksThe BBAQ is a 21-item measure, published by the US Centers for Disease Control and Prevention (CDC), assessing the following barriers to physical activity: 1) lack of time, 2) social influence, 3) lack of energy, 4) lack of willpower, 5) fear of injury, 6) lack of skill, and 7) lack of resources (eg, recreational facilities, exercise equipment). Each domain contains 3 items, with a total score range of 0 to 63. Respondents rate the degree of activity interference on a 4-point scale, ranging from 0 = very unlikely to 3 = very likely. This outcome explores lack of energy category (range of 0-9), and we calculated the change in score from baseline to 8 weeks.
Change in Barriers to Being Active Quiz Score- Lack of WillpowerChange in score from Baseline to 8 weeksThe BBAQ is a 21-item measure, published by the US Centers for Disease Control and Prevention (CDC), assessing the following barriers to physical activity: 1) lack of time, 2) social influence, 3) lack of energy, 4) lack of willpower, 5) fear of injury, 6) lack of skill, and 7) lack of resources (eg, recreational facilities, exercise equipment). Each domain contains 3 items, with a total score range of 0 to 63. Respondents rate the degree of activity interference on a 4-point scale, ranging from 0 = very unlikely to 3 = very likely. This outcome explores lack of will power category (range of 0-9), and we calculated the change in score from baseline to 8 weeks.
Change in Barriers to Being Active Quiz Score - Fear of InjuryChange in score from Baseline to 8 weeksThe BBAQ is a 21-item measure, published by the US Centers for Disease Control and Prevention (CDC), assessing the following barriers to physical activity: 1) lack of time, 2) social influence, 3) lack of energy, 4) lack of willpower, 5) fear of injury, 6) lack of skill, and 7) lack of resources (eg, recreational facilities, exercise equipment). Each domain contains 3 items, with a total score range of 0 to 63. Respondents rate the degree of activity interference on a 4-point scale, ranging from 0 = very unlikely to 3 = very likely. This outcome explores fear of injury category (range of 0-9), and we calculated the change in score from baseline to 8 weeks.
Change in Barriers to Being Active Quiz Score - Lack of SkillChange in score from Baseline to 8 weeksThe BBAQ is a 21-item measure, published by the US Centers for Disease Control and Prevention (CDC), assessing the following barriers to physical activity: 1) lack of time, 2) social influence, 3) lack of energy, 4) lack of willpower, 5) fear of injury, 6) lack of skill, and 7) lack of resources (eg, recreational facilities, exercise equipment). Each domain contains 3 items, with a total score range of 0 to 63. Respondents rate the degree of activity interference on a 4-point scale, ranging from 0 = very unlikely to 3 = very likely. This outcome explores lack of skill category (range of 0-9), and we calculated the change in score from baseline to 8 weeks.
Change in Barriers to Being Active Quiz Score - Lack of ResourcesChange in score from Baseline to 8 weeksThe BBAQ is a 21-item measure, published by the US Centers for Disease Control and Prevention (CDC), assessing the following barriers to physical activity: 1) lack of time, 2) social influence, 3) lack of energy, 4) lack of willpower, 5) fear of injury, 6) lack of skill, and 7) lack of resources (eg, recreational facilities, exercise equipment). Each domain contains 3 items, with a total score range of 0 to 63. Respondents rate the degree of activity interference on a 4-point scale, ranging from 0 = very unlikely to 3 = very likely. This outcome explores lack of resources category (range of 0-9), and we calculated the change in score from baseline to 8 weeks.
Change in SF-12 Scores - Mental Composite ScoreChange in score from Baseline to 8 weeksThe Medical Outcomes Study Short Form-12 (SF-12) will be used to measure quality of life. This is an instrument which has been used in multiple cardiac studies in the past. (SF-12 Mental Composite Score and Physical Composite Score Range: 0-100 each). Change was calculated by subtracting the score at baseline from the score at 8 weeks. Higher scores indicate higher level of health related QoL.
Change in BRFSS- Vegetable ModuleChange in # of vegetables consumed/day from Baseline to 8 weeksMeasure Description: The CDC's BRFSS Fruit and Vegetable Module is a brief questionnaire about frequency of eating different types of fruits and vegetables. It assesses the frequency of consumption of 100% fruit juice, fruit, beans (legumes), dark green vegetables, orange vegetables, and other vegetables over the past month. The outcome measure is the number of vegetables consumed per day.
Change in HADS-D ScoresChange in score from Baseline to 8 weeksThe Hospital Anxiety and Depression Scale will be used to measure depression and anxiety. This is a well-validated scale with few somatic symptom items that can confound mood/anxiety assessment in medically-ill patients.(Range: 0-21). Change was calculated by subtracting the score at baseline from the score at 8 weeks. Higher scores indicate worse outcome (i.e. greater levels of depression).
Physical Activity Adherence (Actigraph)Change in physical activity level from baseline to 8 weeksActiGraph GT3X+ accelerometers are validated as measures of physical activity and have been used in numerous studies of physical activity in patients with medical illness. In this trial, participants will wear the accelerometer to assess the feasibility of doing so and to ensure adequate capture of physical activity.

Countries

United States

Participant flow

Participants by arm

ArmCount
Intervention Arm: PP-MI
Participants will complete an 8-week group physical activity and positive psychology program, in which they will complete exercises related to increasing positive emotions and physical activity during and between the group sessions. They will track their activity (steps) and set personalized physical activity goals each week, as complete a group walk or indoor exercise during the group sessions. We will ask questions about participants' health and health behaviors, and ask them to wear a physical activity monitor at the beginning and end of the program. Intervention arm: PP-MI: The positive psychology exercises include gratitude-based activities, strengths-based activities, and meaning-based activities. The physical activity goal setting exercises include the following topics: health benefits, social resources, and neighborhood walkability.
8
Total8

Baseline characteristics

CharacteristicIntervention Arm: PP-MI
Age, Categorical
<=18 years
0 Participants
Age, Categorical
>=65 years
3 Participants
Age, Categorical
Between 18 and 65 years
5 Participants
Barriers to Being Active Quiz- Lack of Time Scores2.0 score on a scale
STANDARD_DEVIATION 2.5
Barriers to Being Active Quiz Score - Fear of Injury1.4 score on a scale
STANDARD_DEVIATION 1.6
Barriers to Being Active Quiz Score- Lack of Energy1.3 score on a scale
STANDARD_DEVIATION 2.6
Barriers to Being Active Quiz Score - Lack of Resources2.7 score on a scale
STANDARD_DEVIATION 2.8
Barriers to Being Active Quiz Score - Lack of Skill2.7 score on a scale
STANDARD_DEVIATION 0.6
Barriers to Being Active Quiz Score- Lack of Willpower5.9 score on a scale
STANDARD_DEVIATION 0.7
Barriers to Being Active Quiz Score- Social Influence3.4 score on a scale
STANDARD_DEVIATION 2.3
Behavioral Risk Factor Surveillance System Fruit and Vegetable Module - Fruit Category1.2 fruits/day
STANDARD_DEVIATION 1.5
BRFSS- Vegetable Module1.5 vegetable/day
STANDARD_DEVIATION 0.8
Ethnicity (NIH/OMB)
Hispanic or Latino
1 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
7 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
0 Participants
HADS-D Scores4.6 score on a scale
STANDARD_DEVIATION 2.9
Life Orientation Test- Revised Scores11.7 score on a scale
STANDARD_DEVIATION 2.8
National Cancer Institute's Percentage Energy from Fat Screener Scores3.9 number of times consumed per day
STANDARD_DEVIATION 2.8
Physical Activity Adherence (Actigraph)12.5 minutes/week
STANDARD_DEVIATION 10.74
Positive and Negative Affect Schedule Scores36.1 score on a scale
STANDARD_DEVIATION 5
Race (NIH/OMB)
American Indian or Alaska Native
1 Participants
Race (NIH/OMB)
Asian
0 Participants
Race (NIH/OMB)
Black or African American
0 Participants
Race (NIH/OMB)
More than one race
0 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants
Race (NIH/OMB)
Unknown or Not Reported
0 Participants
Race (NIH/OMB)
White
7 Participants
Sex: Female, Male
Female
8 Participants
Sex: Female, Male
Male
0 Participants
SF-12 Scores - Mental Composite Score48.2 score on a scale
STANDARD_DEVIATION 8.2
The Community Healthy Activities Model Program for Seniors Scores14.6 minutes per week
STANDARD_DEVIATION 7.7
The Hospital Anxiety and Depression Scale - Anxiety Scores Scores6.7 score on a scale
STANDARD_DEVIATION 2
The Medical Outcomes Study Short Form-12 Scores - Physical Composite Score41.9 score on a scale
STANDARD_DEVIATION 6
The Neighborhood Environment Walkability Scale-Abbreviated Scores10.7 score on a scale
STANDARD_DEVIATION 1.6

Adverse events

Event typeEG000
affected / at risk
deaths
Total, all-cause mortality
0 / 8
other
Total, other adverse events
1 / 8
serious
Total, serious adverse events
0 / 8

Outcome results

Primary

Number of Participants Completing Objective Physical Activity Measurement

Feasibility will be measured by examining the number of participants who wore Actigraphs with sufficient wear time both at baseline and at follow-up

Time frame: 8 weeks of group sessions

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Intervention Arm: PP-MINumber of Participants Completing Objective Physical Activity Measurement7 Participants
Primary

Number of PP-MI-Based Health Behavior Intervention Exercises Completed

Feasibility will be measured by examining the number of completed exercises.

Time frame: 8 weeks of group sessions

ArmMeasureValue (MEAN)Dispersion
Intervention Arm: PP-MINumber of PP-MI-Based Health Behavior Intervention Exercises Completed7.0 Exercises completedStandard Deviation 0.5
Secondary

Acceptability of Intervention

Acceptability of the intervention was assessed through participants' ratings of each PP and MI exercise. Participants will provide ratings of utility after each exercise, measured on a 10-point Likert scale (0=not at all helpful;10=very helpful). Weekly utility ratings were averaged to provide an overall utility score of the exercises.

Time frame: 8 weeks

ArmMeasureValue (MEAN)Dispersion
Intervention Arm: PP-MIAcceptability of Intervention8.1 score on a scaleStandard Deviation 1
Secondary

Change in Barriers to Being Active Quiz Score - Fear of Injury

The BBAQ is a 21-item measure, published by the US Centers for Disease Control and Prevention (CDC), assessing the following barriers to physical activity: 1) lack of time, 2) social influence, 3) lack of energy, 4) lack of willpower, 5) fear of injury, 6) lack of skill, and 7) lack of resources (eg, recreational facilities, exercise equipment). Each domain contains 3 items, with a total score range of 0 to 63. Respondents rate the degree of activity interference on a 4-point scale, ranging from 0 = very unlikely to 3 = very likely. This outcome explores fear of injury category (range of 0-9), and we calculated the change in score from baseline to 8 weeks.

Time frame: Change in score from Baseline to 8 weeks

ArmMeasureGroupValue (MEAN)Dispersion
Intervention Arm: PP-MIChange in Barriers to Being Active Quiz Score - Fear of InjuryBaseline1.4 score on a scaleStandard Deviation 1.6
Intervention Arm: PP-MIChange in Barriers to Being Active Quiz Score - Fear of Injury8 Weeks1.1 score on a scaleStandard Deviation 1.2
Secondary

Change in Barriers to Being Active Quiz Score- Lack of Energy

The BBAQ is a 21-item measure, published by the US Centers for Disease Control and Prevention (CDC), assessing the following barriers to physical activity: 1) lack of time, 2) social influence, 3) lack of energy, 4) lack of willpower, 5) fear of injury, 6) lack of skill, and 7) lack of resources (eg, recreational facilities, exercise equipment). Each domain contains 3 items, with a total score range of 0 to 63. Respondents rate the degree of activity interference on a 4-point scale, ranging from 0 = very unlikely to 3 = very likely. This outcome explores lack of energy category (range of 0-9), and we calculated the change in score from baseline to 8 weeks.

Time frame: Change in score from Baseline to 8 weeks

ArmMeasureGroupValue (MEAN)Dispersion
Intervention Arm: PP-MIChange in Barriers to Being Active Quiz Score- Lack of EnergyBaseline1.3 score on a scaleStandard Deviation 2.6
Intervention Arm: PP-MIChange in Barriers to Being Active Quiz Score- Lack of Energy8 Weeks1.9 score on a scaleStandard Deviation 2
Secondary

Change in Barriers to Being Active Quiz Score - Lack of Resources

The BBAQ is a 21-item measure, published by the US Centers for Disease Control and Prevention (CDC), assessing the following barriers to physical activity: 1) lack of time, 2) social influence, 3) lack of energy, 4) lack of willpower, 5) fear of injury, 6) lack of skill, and 7) lack of resources (eg, recreational facilities, exercise equipment). Each domain contains 3 items, with a total score range of 0 to 63. Respondents rate the degree of activity interference on a 4-point scale, ranging from 0 = very unlikely to 3 = very likely. This outcome explores lack of resources category (range of 0-9), and we calculated the change in score from baseline to 8 weeks.

Time frame: Change in score from Baseline to 8 weeks

ArmMeasureGroupValue (MEAN)Dispersion
Intervention Arm: PP-MIChange in Barriers to Being Active Quiz Score - Lack of ResourcesBaseline2.7 score on a scaleStandard Deviation 2.8
Intervention Arm: PP-MIChange in Barriers to Being Active Quiz Score - Lack of Resources8 Weeks1.4 score on a scaleStandard Deviation 1.3
Secondary

Change in Barriers to Being Active Quiz Score - Lack of Skill

The BBAQ is a 21-item measure, published by the US Centers for Disease Control and Prevention (CDC), assessing the following barriers to physical activity: 1) lack of time, 2) social influence, 3) lack of energy, 4) lack of willpower, 5) fear of injury, 6) lack of skill, and 7) lack of resources (eg, recreational facilities, exercise equipment). Each domain contains 3 items, with a total score range of 0 to 63. Respondents rate the degree of activity interference on a 4-point scale, ranging from 0 = very unlikely to 3 = very likely. This outcome explores lack of skill category (range of 0-9), and we calculated the change in score from baseline to 8 weeks.

Time frame: Change in score from Baseline to 8 weeks

ArmMeasureGroupValue (MEAN)Dispersion
Intervention Arm: PP-MIChange in Barriers to Being Active Quiz Score - Lack of SkillBaseline2.7 score on a scaleStandard Deviation 0.6
Intervention Arm: PP-MIChange in Barriers to Being Active Quiz Score - Lack of Skill8 Weeks1.1 score on a scaleStandard Deviation 1.2
Secondary

Change in Barriers to Being Active Quiz Score- Lack of Willpower

The BBAQ is a 21-item measure, published by the US Centers for Disease Control and Prevention (CDC), assessing the following barriers to physical activity: 1) lack of time, 2) social influence, 3) lack of energy, 4) lack of willpower, 5) fear of injury, 6) lack of skill, and 7) lack of resources (eg, recreational facilities, exercise equipment). Each domain contains 3 items, with a total score range of 0 to 63. Respondents rate the degree of activity interference on a 4-point scale, ranging from 0 = very unlikely to 3 = very likely. This outcome explores lack of will power category (range of 0-9), and we calculated the change in score from baseline to 8 weeks.

Time frame: Change in score from Baseline to 8 weeks

ArmMeasureGroupValue (MEAN)Dispersion
Intervention Arm: PP-MIChange in Barriers to Being Active Quiz Score- Lack of WillpowerBaseline5.9 score on a scaleStandard Deviation 0.7
Intervention Arm: PP-MIChange in Barriers to Being Active Quiz Score- Lack of Willpower8 Weeks2.1 score on a scaleStandard Deviation 1.3
Secondary

Change in Barriers to Being Active Quiz Score- Social Influence

The BBAQ is a 21-item measure, published by the US Centers for Disease Control and Prevention (CDC), assessing the following barriers to physical activity: 1) lack of time, 2) social influence, 3) lack of energy, 4) lack of willpower, 5) fear of injury, 6) lack of skill, and 7) lack of resources (eg, recreational facilities, exercise equipment). Each domain contains 3 items, with a total score range of 0 to 63. Respondents rate the degree of activity interference on a 4-point scale, ranging from 0 = very unlikely to 3 = very likely. This outcome explores social influence category (range of 0-9), and we calculated the change in score from baseline to 8 weeks.

Time frame: Change in score from Baseline to 8 weeks

ArmMeasureGroupValue (MEAN)Dispersion
Intervention Arm: PP-MIChange in Barriers to Being Active Quiz Score- Social InfluenceBaseline3.4 score on a scaleStandard Deviation 2.3
Intervention Arm: PP-MIChange in Barriers to Being Active Quiz Score- Social Influence8 Weeks2.3 score on a scaleStandard Deviation 1.9
Secondary

Change in BRFSS- Vegetable Module

Measure Description: The CDC's BRFSS Fruit and Vegetable Module is a brief questionnaire about frequency of eating different types of fruits and vegetables. It assesses the frequency of consumption of 100% fruit juice, fruit, beans (legumes), dark green vegetables, orange vegetables, and other vegetables over the past month. The outcome measure is the number of vegetables consumed per day.

Time frame: Change in # of vegetables consumed/day from Baseline to 8 weeks

ArmMeasureGroupValue (MEAN)Dispersion
Intervention Arm: PP-MIChange in BRFSS- Vegetable ModuleBaseline1.5 vegetable/dayStandard Deviation 0.8
Intervention Arm: PP-MIChange in BRFSS- Vegetable Module8 Weeks1.9 vegetable/dayStandard Deviation 0.7
Secondary

Change in HADS-D Scores

The Hospital Anxiety and Depression Scale will be used to measure depression and anxiety. This is a well-validated scale with few somatic symptom items that can confound mood/anxiety assessment in medically-ill patients.(Range: 0-21). Change was calculated by subtracting the score at baseline from the score at 8 weeks. Higher scores indicate worse outcome (i.e. greater levels of depression).

Time frame: Change in score from Baseline to 8 weeks

ArmMeasureGroupValue (MEAN)Dispersion
Intervention Arm: PP-MIChange in HADS-D ScoresBaseline4.6 score on a scaleStandard Deviation 2.9
Intervention Arm: PP-MIChange in HADS-D Scores8 Weeks2.4 score on a scaleStandard Deviation 1.8
Secondary

Change in SF-12 Scores - Mental Composite Score

The Medical Outcomes Study Short Form-12 (SF-12) will be used to measure quality of life. This is an instrument which has been used in multiple cardiac studies in the past. (SF-12 Mental Composite Score and Physical Composite Score Range: 0-100 each). Change was calculated by subtracting the score at baseline from the score at 8 weeks. Higher scores indicate higher level of health related QoL.

Time frame: Change in score from Baseline to 8 weeks

ArmMeasureGroupValue (MEAN)Dispersion
Intervention Arm: PP-MIChange in SF-12 Scores - Mental Composite ScoreBaseline48.2 score on a scaleStandard Deviation 8.2
Intervention Arm: PP-MIChange in SF-12 Scores - Mental Composite Score8 Weeks54.2 score on a scaleStandard Deviation 8.2
Secondary

Changes in Barriers to Being Active Quiz- Lack of Time Scores

The BBAQ is a 21-item measure, published by the US Centers for Disease Control and Prevention (CDC), assessing the following barriers to physical activity: 1) lack of time, 2) social influence, 3) lack of energy, 4) lack of willpower, 5) fear of injury, 6) lack of skill, and 7) lack of resources (eg, recreational facilities, exercise equipment). Each domain contains 3 items, with a total score range of 0 to 63. Respondents rate the degree of activity interference on a 4-point scale, ranging from 0 = very unlikely to 3 = very likely. This outcome explores lack of time category (range of 0-9), and we calculated the change in score from baseline to 8 weeks.

Time frame: Baseline and 8 weeks

ArmMeasureGroupValue (MEAN)Dispersion
Intervention Arm: PP-MIChanges in Barriers to Being Active Quiz- Lack of Time ScoresBaseline2.0 score on a scaleStandard Deviation 2.5
Intervention Arm: PP-MIChanges in Barriers to Being Active Quiz- Lack of Time Scores8 Weeks2.3 score on a scaleStandard Deviation 2
Secondary

Changes in Behavioral Risk Factor Surveillance System Fruit and Vegetable Module - Fruit Category

Measure Description: The CDC's BRFSS Fruit and Vegetable Module is a brief questionnaire about frequency of eating different types of fruits and vegetables. It assesses the frequency of consumption of 100% fruit juice, fruit, beans (legumes), dark green vegetables, orange vegetables, and other vegetables over the past month. The outcome measure is the number of fruits consumed per day.

Time frame: Change in # of fruits consumed/day from Baseline to 8 weeks

ArmMeasureGroupValue (MEAN)Dispersion
Intervention Arm: PP-MIChanges in Behavioral Risk Factor Surveillance System Fruit and Vegetable Module - Fruit CategoryBaseline1.2 fruits/dayStandard Deviation 1.5
Intervention Arm: PP-MIChanges in Behavioral Risk Factor Surveillance System Fruit and Vegetable Module - Fruit Category8 Weeks1.1 fruits/dayStandard Deviation 0.9
Secondary

Changes in Life Orientation Test- Revised Scores

Life Orientation Test-Revised (LOT-R) is a well-validated 6-item instrument used to measure dispositional optimism. (Range: 0-24) Change was calculated by subtracting the score at baseline from the score at 8 weeks. Higher scores indicate higher levels of optimism.

Time frame: Change in dispositional optimism from baseline to 8 weeks

ArmMeasureGroupValue (MEAN)Dispersion
Intervention Arm: PP-MIChanges in Life Orientation Test- Revised ScoresBaseline11.7 score on a scaleStandard Deviation 2.8
Intervention Arm: PP-MIChanges in Life Orientation Test- Revised Scores8 Weeks10.1 score on a scaleStandard Deviation 3.1
Secondary

Changes in National Cancer Institute's Percentage Energy From Fat Screener Scores

The National Cancer Institute's Percentage Energy from Fat Screen is a brief questionnaire that estimates people's typical percentage of energy derived from eating common fat-containing foods, as fat content is related to metabolic syndrome progression. The questionnaire converts an individual's responses to an estimate of that individual's percentage energy from fat. Higher scores indicate higher fat consumption.

Time frame: Change in number of times fat is consumed per day from Baseline to 8 weeks

ArmMeasureGroupValue (MEAN)Dispersion
Intervention Arm: PP-MIChanges in National Cancer Institute's Percentage Energy From Fat Screener ScoresBaseline3.9 # of times fat consumed/dayStandard Deviation 2.8
Intervention Arm: PP-MIChanges in National Cancer Institute's Percentage Energy From Fat Screener Scores8 Weeks3.4 # of times fat consumed/dayStandard Deviation 1.1
Secondary

Changes in Positive and Negative Affect Schedule Scores

The positive affect items on the Positive and Negative Affect Schedule (PANAS), a well-validated scale used in other intervention trials and in patients with HF, will be used to measure positive affect. (Range: 10-50). Change was calculated by subtracting the score at baseline from the score at 8 weeks. Higher scores indicate higher levels of positive affect.

Time frame: Change in score from Baseline to 8 weeks

ArmMeasureGroupValue (MEAN)Dispersion
Intervention Arm: PP-MIChanges in Positive and Negative Affect Schedule ScoresBaseline36.1 score on a scaleStandard Deviation 5
Intervention Arm: PP-MIChanges in Positive and Negative Affect Schedule Scores8 Weeks40.7 score on a scaleStandard Deviation 5.3
Secondary

Changes in The Community Healthy Activities Model Program for Seniors Scores

CHAMP is a self-report questionnaire that assesses weekly frequency and duration of a variety of lifestyle physical activities that are meaningful and appropriate for older adults. It includes activities of various intensities (from light to vigorous) such as walking, running, hiking, swimming, bicycling, dancing, tennis, aerobics, yoga/tai chi, gardening, and housework. The activities are assessed in min/week.

Time frame: Change in score from Baseline to 8 weeks

ArmMeasureGroupValue (MEAN)Dispersion
Intervention Arm: PP-MIChanges in The Community Healthy Activities Model Program for Seniors ScoresBaseline14.6 minutes per weekStandard Deviation 7.7
Intervention Arm: PP-MIChanges in The Community Healthy Activities Model Program for Seniors Scores8 Weeks23.1 minutes per weekStandard Deviation 3.6
Secondary

Changes in The HADS-A Scores

The Hospital Anxiety and Depression Scale will be used to measure depression and anxiety. This is a well-validated scale with few somatic symptom items that can confound mood/anxiety assessment in medically-ill patients. (Range:0-21) Change was calculated by subtracting the score at baseline from the score at 8 weeks. Higher scores indicate higher levels of anxiety.

Time frame: Change in score from Baseline to 8 weeks

ArmMeasureGroupValue (MEAN)Dispersion
Intervention Arm: PP-MIChanges in The HADS-A ScoresBaseline6.7 score on a scaleStandard Deviation 2
Intervention Arm: PP-MIChanges in The HADS-A Scores8 Weeks5.6 score on a scaleStandard Deviation 2.8
Secondary

Changes in The Medical Outcomes Study Short Form-12 Scores - Physical Composite Score

The Medical Outcomes Study Short Form-12 (SF-12) will be used to measure quality of life. This is an instrument which has been used in multiple cardiac studies in the past. (SF-12 Mental Composite Score and Physical Composite Score Range: 0-100 each). Change was calculated by subtracting the score at baseline from the score at 8 weeks. Higher scores indicate higher level of health related QoL.

Time frame: Change in score from Baseline to 8 weeks

ArmMeasureGroupValue (MEAN)Dispersion
Intervention Arm: PP-MIChanges in The Medical Outcomes Study Short Form-12 Scores - Physical Composite ScoreBaseline41.9 score on a scaleStandard Deviation 6
Intervention Arm: PP-MIChanges in The Medical Outcomes Study Short Form-12 Scores - Physical Composite Score8 Weeks44.6 score on a scaleStandard Deviation 9.9
Secondary

Changes in The Neighborhood Environment Walkability Scale-Abbreviated Scores

Measure Description: NEWS is a 98-question instrument that assesses the perception of neighborhood design features related to physical activity. NEWS-A is an abbreviated version and will be used to measure residents' perceptions of neighborhood design related to physical activity, including places for walking and cycling, aesthetics, traffic hazards, and crime (Range: 16-64). Higher scores indicate greater perceived walkability.

Time frame: Change in score from Baseline to 8 weeks

ArmMeasureGroupValue (MEAN)Dispersion
Intervention Arm: PP-MIChanges in The Neighborhood Environment Walkability Scale-Abbreviated ScoresBaseline10.7 score on a scaleStandard Deviation 1.6
Intervention Arm: PP-MIChanges in The Neighborhood Environment Walkability Scale-Abbreviated Scores8 Weeks10.8 score on a scaleStandard Deviation 1.8
Secondary

Physical Activity Adherence (Actigraph)

ActiGraph GT3X+ accelerometers are validated as measures of physical activity and have been used in numerous studies of physical activity in patients with medical illness. In this trial, participants will wear the accelerometer to assess the feasibility of doing so and to ensure adequate capture of physical activity.

Time frame: Change in physical activity level from baseline to 8 weeks

ArmMeasureGroupValue (MEAN)Dispersion
Intervention Arm: PP-MIPhysical Activity Adherence (Actigraph)Baseline12.5 minutes/weekStandard Deviation 10.74
Intervention Arm: PP-MIPhysical Activity Adherence (Actigraph)Week 840.9 minutes/weekStandard Deviation 70.6

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026