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MAP to Health Pilot Study: A Physical Activity Intervention for Midlife Adults

Development and Proof-of-Concept Trial of a Meaning- and Theory-based Physical Activity Intervention

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05332145
Acronym
MAP
Enrollment
35
Registered
2022-04-18
Start date
2022-11-04
Completion date
2023-05-04
Last updated
2023-12-06

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

Conditions

Physical Inactivity

Brief summary

The study has two aims: (1) to develop and examine the acceptability of the technological and theoretical frameworks of MAP to Health and (2) to determine whether MAP to Health is related to changes in theoretically identified mechanisms of behavior change (meaning salience, basic psychological needs satisfaction, and internal motivation). In an exploratory aim, the study will assess how the intervention and mechanisms of change are related to changes in physical activity. Participants will be adults in midlife (ages 40-64) who are insufficiently active, are interested in increasing physical activity, do not have contraindications to engaging in physical activity, and are patients in a large healthcare system in the Midwest.

Interventions

BEHAVIORALMAP to Health

In Phase 1, participants will complete the web-based interview and Aim 1 measures, assessing acceptability and usability of the intervention. The investigators will review whether the intervention appropriately gathers information needed to program theory-based, personalized text messages. After completing the measures, a list of text messages for that participant will be generated and sent to the participant for review. Participants will review the text messages and rate the extent to which the messages are personalized. In Phase 2, the investigators will conduct a proof-of-concept pilot trial in which participants will complete a 4-week pretest monitoring period and an 8-week pilot trial of the intervention, with assessments of Self-Determination Theory mechanisms and meaning salience at pretest (-4 weeks), baseline (0 weeks), midpoint (4 weeks) and posttest (8 weeks). In addition, participants will wear accelerometers to assess physical activity during the 12 weeks.

Sponsors

National Institute on Aging (NIA)
CollaboratorNIH
HealthPartners Institute
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Intervention model description

In Phase 1, the investigators will develop the MAP to Health web-based interview that will be used to explore what is particularly meaningful to participants, how physical activity is consistent with those goals, and what activities patients plan to engage in. Participants (N=12) will complete the interview and rate the ease of use, usefulness, intention to use, and theoretical fidelity of the intervention. In Phase 2, the investigators will conduct a proof-of-concept pilot trial using a double-pretest single group design. Participants (N=35) will complete a 4-week pretest monitoring period and an 8-week pilot trial of the intervention, with assessments of Self-Determination Theory mechanisms and meaning salience at pretest (-4 weeks), baseline (0 weeks), midpoint (4 weeks) and posttest (8 weeks). In addition, participants will wear accelerometers to assess physical activity during the 12 weeks.

Eligibility

Sex/Gender
ALL
Age
40 Years to 64 Years
Healthy volunteers
No

Inclusion criteria

* Midlife (ages 40-64 at enrollment) * Able to read and understand English * Insufficiently active (engaging in ≥10 and ≤90 min of physical activity/week) * Intention to increase physical activity in the next 30 days * Has consistent access to a phone with text-messaging capability

Exclusion criteria

* Greater than minimal risk to starting a physical activity program (Physical Activity Readiness Questionnaire score \> 0) * Body Mass Index (BMI)≥ 40 * Currently pregnant * Has opted out of research * Diagnosis of metastatic cancer or cardiovascular disease * Residing in a nursing home or long-term care facility * Cognitive or psychiatric conditions that preclude completion of questionnaires, including dementia diagnosis * Diagnosis of severe psychiatric disorder (e.g., Bipolar Disorder, Schizophrenia) * Diagnosis of substance use disorder or AUDIT-C62 \>3 for women or \>4 for men

Design outcomes

Primary

MeasureTime frameDescription
Meaning Salience12 weeksThe Meaning Awareness Scale is a 6-item self-report measure that assesses meaning salience. Participants rate the extent to which they were aware of meaning over the past day (e.g, I was aware of the meaning in my life on a 7-point Likert type scale ranging from 1 (rarely) to 7 (very often). Items are averaged for a total score (range, 1-7). Participants complete the scale on three random days during each of the four assessment periods and total scores are averaged across those three days. A higher score signifies greater meaning salience, a better outcome.
Basic Psychological Needs Satisfaction12 weeksThe Psychological Needs Satisfaction in Exercise Scale is a self-report measure used to assess participants' satisfaction of three basic psychological needs (autonomy, competence, and relatedness) in exercise. The scale has 18 items that participants rate on a 6-point Likert-type scale ranging from 1 (false) to 6 (true). Items are averaged within each subscale (autonomy, competence, and relatedness) with possible scores ranging from 1-6. Higher scores indicate greater satisfaction of autonomy, competence and relatedness, a better outcome.
Autonomous Motivation12 weeks• Autonomous motivation was measured using the Behavioral Regulations in Exercise Questionnaire, version 4. The 28-item self-report measure assesses motivations for exercise on the self-determination theory continuum. There are 7 subscales with 4 items each (intrinsic, integrated, identified, introjected - approach, introjected - avoidance, external, and amotivation). Items are summed within each subscale (total score range, 4-28). The subscales were combined using a bifurcation approach, where subscale scores were averaged into two subscales: autonomous (intrinsic, integrated, and identified, total score range 4-28) and controlled motivation (introjected-approach, introjected - avoidance, and external, total score range, 4-28). Higher scores on the autonomous subscale indicate greater internalized motivation, a positive outcome, whereas higher scores on the controlled subscale indicates greater external motivation, a negative outcome.
Technology Acceptancewithin 1 week post-interventionParticipants answered 10 questions rating the extent to which they found the MAP to Health intervention easy to use (4 items) and useful (4-items) and their intentions to use the intervention in the future (2 items). Survey questions were based on previous research and modified for the purposes of this study. Participants rated each item on a scale from 1 (strongly disagree) to 5 (strongly agree). Items were averaged within each subscale, with possible total scores ranging from 1-5. A higher score represents greater technology acceptance, a better outcome.

Countries

United States

Participant flow

Participants by arm

ArmCount
Intervention Testing
Participants will complete a 4-week pretest monitoring period and an 8-week pilot trial of the intervention, with assessments of Self-Determination Theory mechanisms and meaning salience at pretest (-4 weeks), baseline (0 weeks), midpoint (4 weeks) and posttest (8 weeks). In addition, participants will wear accelerometers to assess physical activity during the 12 week period.
35
Total35

Baseline characteristics

CharacteristicIntervention Testing
Age, Categorical
<=18 years
0 Participants
Age, Categorical
>=65 years
0 Participants
Age, Categorical
Between 18 and 65 years
35 Participants
Autonomous Motivation19.78 score on a scale
STANDARD_DEVIATION 5.5
Basic Psychological Needs Satisfaction
Autonomy
5.2 score on a scale
STANDARD_DEVIATION 0.77
Basic Psychological Needs Satisfaction
Competence
4.3 score on a scale
STANDARD_DEVIATION 1.27
Basic Psychological Needs Satisfaction
Relatedness
3.7 score on a scale
STANDARD_DEVIATION 1.49
Ethnicity (NIH/OMB)
Hispanic or Latino
2 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
33 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
0 Participants
Meaning Salience5.09 score on a scale
STANDARD_DEVIATION 1.48
Race (NIH/OMB)
American Indian or Alaska Native
1 Participants
Race (NIH/OMB)
Asian
7 Participants
Race (NIH/OMB)
Black or African American
3 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
1 Participants
Race (NIH/OMB)
White
23 Participants
Sex: Female, Male
Female
27 Participants
Sex: Female, Male
Male
8 Participants

Adverse events

Event typeEG000
affected / at risk
deaths
Total, all-cause mortality
0 / 35
other
Total, other adverse events
0 / 35
serious
Total, serious adverse events
0 / 35

Outcome results

Primary

Autonomous Motivation

• Autonomous motivation was measured using the Behavioral Regulations in Exercise Questionnaire, version 4. The 28-item self-report measure assesses motivations for exercise on the self-determination theory continuum. There are 7 subscales with 4 items each (intrinsic, integrated, identified, introjected - approach, introjected - avoidance, external, and amotivation). Items are summed within each subscale (total score range, 4-28). The subscales were combined using a bifurcation approach, where subscale scores were averaged into two subscales: autonomous (intrinsic, integrated, and identified, total score range 4-28) and controlled motivation (introjected-approach, introjected - avoidance, and external, total score range, 4-28). Higher scores on the autonomous subscale indicate greater internalized motivation, a positive outcome, whereas higher scores on the controlled subscale indicates greater external motivation, a negative outcome.

Time frame: 12 weeks

Population: After enrollment of 35 study participants, one participant withdrew and one was lost to follow-up.

ArmMeasureValue (MEDIAN)Dispersion
MAP to Health Intervention: Phase 2Autonomous Motivation21.43 score on a scaleStandard Deviation 5.06
Primary

Basic Psychological Needs Satisfaction

The Psychological Needs Satisfaction in Exercise Scale is a self-report measure used to assess participants' satisfaction of three basic psychological needs (autonomy, competence, and relatedness) in exercise. The scale has 18 items that participants rate on a 6-point Likert-type scale ranging from 1 (false) to 6 (true). Items are averaged within each subscale (autonomy, competence, and relatedness) with possible scores ranging from 1-6. Higher scores indicate greater satisfaction of autonomy, competence and relatedness, a better outcome.

Time frame: 12 weeks

ArmMeasureGroupValue (MEAN)Dispersion
MAP to Health Intervention: Phase 2Basic Psychological Needs SatisfactionCompetence5.0 score on a scaleStandard Deviation 0.86
MAP to Health Intervention: Phase 2Basic Psychological Needs SatisfactionAutonomy5.7 score on a scaleStandard Deviation 0.6
MAP to Health Intervention: Phase 2Basic Psychological Needs SatisfactionRelatedness4.3 score on a scaleStandard Deviation 1.6
Primary

Meaning Salience

The Meaning Awareness Scale is a 6-item self-report measure that assesses meaning salience. Participants rate the extent to which they were aware of meaning over the past day (e.g, I was aware of the meaning in my life on a 7-point Likert type scale ranging from 1 (rarely) to 7 (very often). Items are averaged for a total score (range, 1-7). Participants complete the scale on three random days during each of the four assessment periods and total scores are averaged across those three days. A higher score signifies greater meaning salience, a better outcome.

Time frame: 12 weeks

ArmMeasureValue (MEAN)Dispersion
MAP to Health Intervention: Phase 2Meaning Salience5.61 score on a scaleStandard Deviation 1.22
Primary

Technology Acceptance

Participants answered 10 questions rating the extent to which they found the MAP to Health intervention easy to use (4 items) and useful (4-items) and their intentions to use the intervention in the future (2 items). Survey questions were based on previous research and modified for the purposes of this study. Participants rated each item on a scale from 1 (strongly disagree) to 5 (strongly agree). Items were averaged within each subscale, with possible total scores ranging from 1-5. A higher score represents greater technology acceptance, a better outcome.

Time frame: within 1 week post-intervention

ArmMeasureGroupValue (MEAN)Dispersion
MAP to Health Intervention: Phase 2Technology AcceptanceUsability4.28 score on a scaleStandard Deviation 0.64
MAP to Health Intervention: Phase 2Technology AcceptanceEase of Use4.32 score on a scaleStandard Deviation 0.76
MAP to Health Intervention: Phase 2Technology AcceptanceIntent to Use3.77 score on a scaleStandard Deviation 1.29

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