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Evaluation of the Healthy Lifestyle Program on Cognitive Outcomes

Evaluation of the Healthy Lifestyle Program on Cognitive Outcomes

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03926481
Enrollment
6
Registered
2019-04-24
Start date
2019-07-10
Completion date
2020-03-20
Last updated
2022-08-03

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

Conditions

Obesity

Keywords

weight loss, cognition, sarcopenia, obesity, lifestyle

Brief summary

The goal of this study is to conduct a program of pilot research aimed at evaluating the effect of an intensive lifestyle intervention on cognitive functioning in older adults with obesity and or obesity and sarcopenia.

Detailed description

Detailed Description: The national epidemic of obesity is also affecting older adults, and is associated with an increased risk of disability, nursing home placement and early mortality. The overarching goal of this study is to conduct a program of pilot research aimed at evaluating the effect of a intensive lifestyle intervention on cognitive functioning in order adults with obesity and or obesity and sarcopenia. While some degree of cognitive decline is common during the normal aging process, epidemiological evidence suggests that obesity can promote its acceleration. It is unclear the effect that intensive lifestyle changes could have on cognitive functioning in older adults with obesity. Study Timeline: May 2019 to May 2023 Goal: Conduct a study to evaluate the effects that intensive lifestyle program has on cognitive functioning in older adults with obesity and or obesity and sarcopenia. Participation Duration: Participants will meet weekly for 17 weeks. Cognitive assessments will take place at baseline and 17 weeks.

Interventions

BEHAVIORALEvaluate Healthy Lifestyle Program on cognitive outcomes

The healthy lifestyle program will be delivered once a week for 17 weeks as part as regular clinical care. It will include an group classes taught by health coaches and dieticians. These classes will focus on diet, exercise, and behavior modification. We plan 2 cohorts of 15 subjects (n=30). In-person research assistant-led assessments will occur at baseline and 17 weeks.

Sponsors

Dartmouth-Hitchcock Medical Center
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* English Speaking * Age ≥65 years * Body Composition Body Fat \>25% for Men * Body Composition Body Fat \>30% for Women * Participating in the Dartmouth Hitchcock Weight and Wellness Center (WWC) Healthy Lifestyle Program (HLP) * Willing and able to give informed consent

Exclusion criteria

* Unable to perform measures * Individuals unwilling/unable to provide consent * Severe mental or life-threatening illness * History of bariatric surgery

Design outcomes

Primary

MeasureTime frameDescription
Change in Prospective and Retrospective Memory Questionnaire (PRMQ)Baseline and 17 weeksPRMQ is a questionnaire about daily memory difficulties. Higher scores represent worse outcomes. Total score ranges from 0-64.
Change from baseline Subjective Health Status (PROMIS) at 17 weeksBaseline and 17 weeksPatient Reported Outcomes Measurement Information Systems (PROMIS) Global Short Form. PROMIS is a 10-item instrument capturing physical, mental and social aspects of quality of life having undergone quantitative appraisal and is non-proprietary. Higher score indicated more positive perceptions of overall health.
Change in Behavior Rating Inventory of Executive Function (BRIEF-A)Baseline and 17 weeksBehavior Rating Inventory of Executive Function (BREIF-A) is used to evaluate executive functioning.This questionnaire consist of 75 items on which the patient's symptoms are rated on a 3-point Likert scale. The questionnaire provides a Global Executive Composite score (range 75-225) and two index scores: the Behavioral Regulation Index (range 30-90) and the Metacognitive Index (range 40-120) in addition to nine subscales: Inhibit (range 8-24), Shift (range 6-18), Emotional control (range 10-30), Self-monitor (range 6-18), Initiate (range 8-24), Working memory (range 8-24), Plan/organize (range 10-30), Task monitor (range 6-18) and Organization of materials (range 8-24). Higher scores indicate more executive difficulties.
Change in grip strengthBaseline and 17 weeksAssessed by a Jamar dynamometer. Sensor-based Thera-bands will measure data on strength change. A higher score represents a better outcome.
Change in 5 times Sit-to-Stand (STS)Baseline and 17 weeksSTS measures lower limb strength (minimal change 2.3 s). A higher score represents a better outcome.
Change in Six-Minute Walk Test (6MWT)Baseline and 17 weeksA surrogate for cardiovascular fitness that measures distance (normal 400-700m) related to function. A clinically important difference is 50-55m
Change in weight in kgBaseline and 17 weeksChange in weight in kg
Change in body mass index (BMI) in kg/m^2Baseline and 17 weeksChange in body mass index (BMI) in kg/m\^2
Change in subject processing speedBaseline and 17 weeksSingle Digit Modalities Test: Measure of cognition/processing speed. Score range 0 to 110. A higher score represents a better outcome.
Change in language functionBaseline and 17 weeksBoston Naming Test (BNT) is used to evaluate language function. Score range:0-42; higher score indicates better performance.
Change in subject cognitionBaseline and 17 weeksVerbal fluency test is used to evaluate language function. Performance will be identified via the total number of appropriate words responded on each of the task. Higher score indicates better performance.
Change in subject executive functionBaseline and 17 weeksStroop test is used to assess executive function. Higher score indicates better performance. Raw score range: 0-300.
Change in speed processingBaseline and 17 weeksTrail making Test-A&B is used to assess information processing speed. Shorter time indicates better performance.
Change in subject memoryBaseline and 17 weeksCalifornia Verbal Learning Test II (CVLT-II) Trials 1-5 Total raw score (range: 0-80; higher values represent a better outcome)
Change in Brief Visuospatial Memory Test-Revised (BVMT-R)Baseline and 17 weeksBVMT-R is used to evaluate spatial memory ability. Scores range from 0 to 60, with higher values indicating better performance.
Change from baseline Anxiety Symptoms at 17 weeksBaseline and 17 weekswill be assessed using the Generalized Anxiety Disorder-7 (GAD7). The GAD7 scores range from 5-21, with 5-9 indicating mild, 10-14 moderate, and greater than 15 severe anxiety.
Change from baseline Mood Symptoms at 17 weeksBaseline and 17 weeksWill be assessed using the Patient Healthy Questionnaire (PHQ9). The PHQ9 scores range from 0-27, with lower numbers indicating minimal to no depression and higher numbers indicating severe depression.

Secondary

MeasureTime frameDescription
Handedness as measured by Edinburgh Handedness Inventory at BaselineBaselineA self report questionnaire assessing the dominance of one's right or left hand in everyday activities.
Baseline estimated level of intellectual abilityBaselineTest of Premorbid Functioning which results in a total raw score ranging from 0-70, and is normatively scored based on respondents' age resulting in standard scores (mean = 100). Higher values indicate a higher premorbid level of intellect.

Countries

United States

Outcome results

None listed

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