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MOWI Research Pilot

Primary Purpose

Obesity

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Develop & Refine MOWI w/o Amulet
MOWI Weight Loss Maintenance
Develop & Refine MOWI w Fitbit
Develop & Refine MOWI w Fitbit/Protein
Sponsored by
Dartmouth-Hitchcock Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Obesity focused on measuring frail elderly, telemedicine, obesity, rural health, health promotion, weight loss

Eligibility Criteria

65 Years - undefined (Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

All Aims:

  • Age ≥65 years
  • Body Mass Index (BMI) ≥ 30kg/m^2
  • Waist circumference ≥88cm in females or ≥102cm in males

Aims 2 & 3:

  • Have Wi-Fi high speed internet
  • Able to obtain medical clearance from doctor
  • Have less than a 5% weight loss in past 6 months
  • No advanced co-morbidity
  • No exercise restrictions
  • Not involved in other research studies that may interfere with participation

Exclusion Criteria:

  • Severe mental or life-threatening illness
  • Dementia
  • Substance use
  • History of bariatric surgery
  • Suicidal ideation
  • Unable to perform measures
  • Reside in nursing home
  • No advanced co-morbidity
  • No exercise restrictions
  • Not involved in other research studies that may interfere with participation

Aim 4 - had to have completed Aims 2 or 3

Sites / Locations

  • Dartmouth-Hitchcock Medical Center

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Active Comparator

Experimental

Active Comparator

Active Comparator

Arm Label

Develop & Refine MOWI w/o Amulet (2A)

MOWI Weight Loss Maintenance

Develop & Refine MOWI w Fitbit (2B)

Develop & Refine MOWI w Fitbit/Protein (2P)

Arm Description

Develop and refine a mHealth obesity wellness intervention (MOWI) for rural, older, obese adults without the use of Amulet technology.

Evaluate the feasibility, acceptability, and potential effectiveness of an 8-session, tri-weekly, psychosocial skills group intervention to support weight loss maintenance post-MOWI.

Develop and refine a mHealth obesity wellness intervention (MOWI) for rural, older, obese adults with the use of Fitbit technology.

Develop and refine a mHealth obesity wellness intervention (MOWI) for rural, older, obese adults with the use of Fitbit technology augmented by whey protein.

Outcomes

Primary Outcome Measures

Change in Grip Strength
Assessed by a Jamar dynamometer. Sensor-based Thera-bands will measure data on strength change.
Change in 5 Times Sit-to-Stand (STS)
STS measures lower limb strength (minimal change 2.3 s).
Change in Six-Minute Walk Test (6MWT)
A surrogate for cardiovascular fitness that measures distance (normal 400-700m) related to function. A clinically important difference is 50-55m
Change in Gait Speed (m/s)
Gait speed is measured by the time it takes to walk 20 meters. Gait speed predicts disability and mortality (significant change 0.1 m/s).
Change in Late-Life Function and Disability Instrument (LLFDI)
LLFDI consists of a 32-item function and 16-item disability (life-task) scales that correlate with gait speed and lower limb function. Higher points indicate better function. Individual raw scores range from 0 to 80, scaled scores are 0 to 100. Each was assessed at baseline and at 12 weeks. We report the differences between baseline/follow-up. Positive score change reflect improved physical function.

Secondary Outcome Measures

Change in Behavioral Activation (Patient Activation Measure)
Patient Activation Measure (PAM) assesses knowledge, confidence and skill for managing health and grouped into 4 levels revealing insights into attitudes, motivators, behaviors & outcomes. Higher points indicate better activation. Measures are scored 0-100 units. Scores below reflect changes between baseline and follow-up at 12-weeks. A positive change score indicates improvement in activation
Change in Subjective Health Status (PROMIS) Physical
Patient 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 points indicate better health. Raw scores are scaled to 0-100. 50 is the mean, 10 points indicates 1 standard deviation. Positive change scores listed below indicate an improvement in subjective health
Change in Weight in kg
Change in weight in kg
Change in Waist Circumference in cm
Change in waist and hip circumference in cm
Average Steps/Expenditure
Average Steps will be measured over a 12 week period
Community Healthy Activities Model Program for Seniors Physical Activity Questionnaire (CHAMPS) - Change in Number of Activities
CHAMPS is a self-reported tool in older adults that assesses activity levels and types -
Change in Body Composition - Lean Mass
Lean mass was assessed using bioelectrical impedance for 2P and 2B. This technique was not available for MOWI 2A participants and hence not measured
Change in Energy Expenditure
Resting metabolic rate, Change Score (kCal) from Baseline to 12 weeks
Change in Fasting Plasma Glucose
Fasting Plasma Glucose
Change in Participant Satisfaction Questionnaire Score
The Participant Satisfaction Questionnaire is a 12-item questionnaire which measures participant satisfaction with intervention participation using a Likert scale (0-5 point scale: very unsatisfied = 0 to very satisfied = 4). Total scores range 0-60: higher scores indicate greater satisfaction with the intervention.Three additional sub-items ask participants to rate their preference for the frequency of sessions, length of group meetings, and total number of group meetings using a Likert scale (-1 - 1 point scale: too few/too short = -1 to 1 = too much/too long). Each of these three items will be interpreted individually and not included in a summed total score. Additionally, this questionnaire includes 1 open-ended response item where participants are asked to leave any additional comments they may have regarding their level of satisfaction with the intervention.
Change in Credibility and Expectancy Questionnaire Score
The Credibility and Expectancy Questionnaire is a 6-item questionnaire which measures expectancies regarding intervention participation and intervention rationale credibility using a Likert scale (0-10 point scale: responses are anchored to question stems such that, not at all logical/not at all effective/not at all confident/no credibility/not at all comfortable = 0 and very logical/very effective/very confident/high credibility = 10). Total scores range 0-50: higher scores indicate more favorable expectancies regarding participation in the intervention/greater perceived intervention credibility. Additionally, this questionnaire includes 1 open-ended response item that asks participants to leave any additional comments they may have regarding their expectations for the intervention
Community Healthy Activities Model Program for Seniors Physical Activity Questionnaire (CHAMPS) - Change in Number of Not Exercising Activities
CHAMPS is a self-reported tool in older adults that assesses activity levels and types -
Community Healthy Activities Model Program for Seniors Physical Activity Questionnaire (CHAMPS) - Change in Duration
CHAMPS is a self-reported tool in older adults that assesses activity levels and types -
Community Healthy Activities Model Program for Seniors Physical Activity Questionnaire (CHAMPS)
CHAMPS is a self-reported tool in older adults that assesses activity levels and types -
Change in Insulin Level
insulin
Change in C-peptide
C-peptide
Change in C-reactive Protein
C-reactive protein
Change in Tumor Necrosis Factor Alpha
tumor necrosis factor alpha
Change in Interleukin 6
Interleukin 6

Full Information

First Posted
April 3, 2017
Last Updated
November 4, 2022
Sponsor
Dartmouth-Hitchcock Medical Center
Collaborators
National Institute on Aging (NIA)
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1. Study Identification

Unique Protocol Identification Number
NCT03104192
Brief Title
MOWI Research Pilot
Official Title
Mobile Health Obesity Wellness Intervention in Rural Older Adults (MOWI): Research Pilot
Study Type
Interventional

2. Study Status

Record Verification Date
November 2022
Overall Recruitment Status
Completed
Study Start Date
September 1, 2017 (Actual)
Primary Completion Date
January 3, 2019 (Actual)
Study Completion Date
January 11, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Dartmouth-Hitchcock Medical Center
Collaborators
National Institute on Aging (NIA)

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The goal of this study is to conduct a program of pilot research aimed at developing and evaluating a technology-assisted wellness intervention for older adults with obesity.
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. Conventional weight loss programs have the potential to reduce body fat, but are difficult to access for older obese adults due to transportation and mobility challenges. The overarching goal of this study is to conduct a program of pilot research aimed at developing and evaluating a technology assisted wellness intervention for older adults with obesity. Study Timeline: September 2017 to June 2018: Goal: Conduct a pilot study of improving weight and physical function in older adults with obesity. An mHealth Obesity Wellness Intervention (MOWI) will integrate Amulet +/- Fitbi with a weekly individual dietician-led nutritional session, along with twice weekly physical therapist led group exercise session. Participation Duration: Three times weekly for 3 months

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obesity
Keywords
frail elderly, telemedicine, obesity, rural health, health promotion, weight loss

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Two Arm Pilot Study
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
69 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Develop & Refine MOWI w/o Amulet (2A)
Arm Type
Active Comparator
Arm Description
Develop and refine a mHealth obesity wellness intervention (MOWI) for rural, older, obese adults without the use of Amulet technology.
Arm Title
MOWI Weight Loss Maintenance
Arm Type
Experimental
Arm Description
Evaluate the feasibility, acceptability, and potential effectiveness of an 8-session, tri-weekly, psychosocial skills group intervention to support weight loss maintenance post-MOWI.
Arm Title
Develop & Refine MOWI w Fitbit (2B)
Arm Type
Active Comparator
Arm Description
Develop and refine a mHealth obesity wellness intervention (MOWI) for rural, older, obese adults with the use of Fitbit technology.
Arm Title
Develop & Refine MOWI w Fitbit/Protein (2P)
Arm Type
Active Comparator
Arm Description
Develop and refine a mHealth obesity wellness intervention (MOWI) for rural, older, obese adults with the use of Fitbit technology augmented by whey protein.
Intervention Type
Behavioral
Intervention Name(s)
Develop & Refine MOWI w/o Amulet
Other Intervention Name(s)
MOWI 2A
Intervention Description
The mHealth Obesity Wellness Intervention (MOWI) will be informed by the previous Aim (Aim 1) of this proposal. It will consist of a 12-week, 3x/week program of: weekly nutrition counseling; 2x/week group exercise visits. A dietician and physical therapist will lead the in-person sessions. A wave of 8 individuals each will be assessed at 0, 4, 8 and 12 weeks.
Intervention Type
Behavioral
Intervention Name(s)
MOWI Weight Loss Maintenance
Other Intervention Name(s)
MOWI LT
Intervention Description
Participants who successfully completed the initial MOWI program will be offered the opportunity to participate in a 6-month weight management program. This program will consist of 8 group-based skills workshop sessions occurring approximately once monthly (every 3 weeks), which will be 90-120 minutes in length. The overall structure of the program will emphasize the following evidence-based weight management components: Goal setting/action planning, self-monitoring, receiving feedback regarding performance, reviewing relevant goals in the light of feedback, and e. psychological skills for increasing behavioral commitment (acceptance, willingness, thought monitoring, mindful decision making, and values clarification).
Intervention Type
Behavioral
Intervention Name(s)
Develop & Refine MOWI w Fitbit
Other Intervention Name(s)
MOWI 2B-2
Intervention Description
The mHealth Obesity Wellness Intervention (MOWI) will be informed by the previous Aim (Aim 1) of this proposal. It will consist of a 12-week, 3x/week program of: weekly nutrition counseling; 2x/week group exercise visits; and Fitbit to monitor activity. A dietician and physical therapist will lead the in-person sessions. A wave of 8 individuals each will be assessed at 0, 4, 8 and 12 weeks and will also be given Amulet to measure steps, activity type, duration and distance.
Intervention Type
Dietary Supplement
Intervention Name(s)
Develop & Refine MOWI w Fitbit/Protein
Other Intervention Name(s)
MOWI Protein-2
Intervention Description
The mHealth Obesity Wellness Intervention (MOWI) will be informed by the previous Aim (Aim 1) of this proposal. It will consist of a 12-week, 3x/week program of: weekly nutrition counseling; 2x/week group exercise visits; and Fitbit to monitor activity. A dietician and physical therapist will lead the in-person sessions. A wave of 8 individuals each will be assessed at 0, 4, 8 and 12 weeks and will also be given Amulet to measure steps, activity type, duration and distance. We will provide whey protein 3x/week after exercise sessions.
Primary Outcome Measure Information:
Title
Change in Grip Strength
Description
Assessed by a Jamar dynamometer. Sensor-based Thera-bands will measure data on strength change.
Time Frame
Baseline, 12 weeks
Title
Change in 5 Times Sit-to-Stand (STS)
Description
STS measures lower limb strength (minimal change 2.3 s).
Time Frame
Baseline, 12 weeks
Title
Change in Six-Minute Walk Test (6MWT)
Description
A surrogate for cardiovascular fitness that measures distance (normal 400-700m) related to function. A clinically important difference is 50-55m
Time Frame
Baseline, 12 weeks
Title
Change in Gait Speed (m/s)
Description
Gait speed is measured by the time it takes to walk 20 meters. Gait speed predicts disability and mortality (significant change 0.1 m/s).
Time Frame
Baseline, 12 weeks
Title
Change in Late-Life Function and Disability Instrument (LLFDI)
Description
LLFDI consists of a 32-item function and 16-item disability (life-task) scales that correlate with gait speed and lower limb function. Higher points indicate better function. Individual raw scores range from 0 to 80, scaled scores are 0 to 100. Each was assessed at baseline and at 12 weeks. We report the differences between baseline/follow-up. Positive score change reflect improved physical function.
Time Frame
Baseline, 12 weeks
Secondary Outcome Measure Information:
Title
Change in Behavioral Activation (Patient Activation Measure)
Description
Patient Activation Measure (PAM) assesses knowledge, confidence and skill for managing health and grouped into 4 levels revealing insights into attitudes, motivators, behaviors & outcomes. Higher points indicate better activation. Measures are scored 0-100 units. Scores below reflect changes between baseline and follow-up at 12-weeks. A positive change score indicates improvement in activation
Time Frame
Baseline, 12 weeks post study
Title
Change in Subjective Health Status (PROMIS) Physical
Description
Patient 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 points indicate better health. Raw scores are scaled to 0-100. 50 is the mean, 10 points indicates 1 standard deviation. Positive change scores listed below indicate an improvement in subjective health
Time Frame
Baseline, 12-weeks
Title
Change in Weight in kg
Description
Change in weight in kg
Time Frame
Baseline, 12 weeks
Title
Change in Waist Circumference in cm
Description
Change in waist and hip circumference in cm
Time Frame
Baseline, 12 weeks post study
Title
Average Steps/Expenditure
Description
Average Steps will be measured over a 12 week period
Time Frame
Mean steps over 12 week period of time
Title
Community Healthy Activities Model Program for Seniors Physical Activity Questionnaire (CHAMPS) - Change in Number of Activities
Description
CHAMPS is a self-reported tool in older adults that assesses activity levels and types -
Time Frame
Change Score between baseline and 12 weeks
Title
Change in Body Composition - Lean Mass
Description
Lean mass was assessed using bioelectrical impedance for 2P and 2B. This technique was not available for MOWI 2A participants and hence not measured
Time Frame
Baseline, 12 weeks
Title
Change in Energy Expenditure
Description
Resting metabolic rate, Change Score (kCal) from Baseline to 12 weeks
Time Frame
Baseline to 12 weeks
Title
Change in Fasting Plasma Glucose
Description
Fasting Plasma Glucose
Time Frame
Baseline, 12 weeks
Title
Change in Participant Satisfaction Questionnaire Score
Description
The Participant Satisfaction Questionnaire is a 12-item questionnaire which measures participant satisfaction with intervention participation using a Likert scale (0-5 point scale: very unsatisfied = 0 to very satisfied = 4). Total scores range 0-60: higher scores indicate greater satisfaction with the intervention.Three additional sub-items ask participants to rate their preference for the frequency of sessions, length of group meetings, and total number of group meetings using a Likert scale (-1 - 1 point scale: too few/too short = -1 to 1 = too much/too long). Each of these three items will be interpreted individually and not included in a summed total score. Additionally, this questionnaire includes 1 open-ended response item where participants are asked to leave any additional comments they may have regarding their level of satisfaction with the intervention.
Time Frame
Change score from pre/post (baseline - at end of initial MOWI 12 weeks; follow-up at end of Maintenance study 6 months post-end of MOWI))
Title
Change in Credibility and Expectancy Questionnaire Score
Description
The Credibility and Expectancy Questionnaire is a 6-item questionnaire which measures expectancies regarding intervention participation and intervention rationale credibility using a Likert scale (0-10 point scale: responses are anchored to question stems such that, not at all logical/not at all effective/not at all confident/no credibility/not at all comfortable = 0 and very logical/very effective/very confident/high credibility = 10). Total scores range 0-50: higher scores indicate more favorable expectancies regarding participation in the intervention/greater perceived intervention credibility. Additionally, this questionnaire includes 1 open-ended response item that asks participants to leave any additional comments they may have regarding their expectations for the intervention
Time Frame
Baseline (of maintenance intervention) and 6 months (into maintenance) - pre/post
Title
Community Healthy Activities Model Program for Seniors Physical Activity Questionnaire (CHAMPS) - Change in Number of Not Exercising Activities
Description
CHAMPS is a self-reported tool in older adults that assesses activity levels and types -
Time Frame
Change Score between baseline and 12 weeks
Title
Community Healthy Activities Model Program for Seniors Physical Activity Questionnaire (CHAMPS) - Change in Duration
Description
CHAMPS is a self-reported tool in older adults that assesses activity levels and types -
Time Frame
Change Score between baseline and 12 weeks
Title
Community Healthy Activities Model Program for Seniors Physical Activity Questionnaire (CHAMPS)
Description
CHAMPS is a self-reported tool in older adults that assesses activity levels and types -
Time Frame
Change in KCal between baseline and 12 weeks
Title
Change in Insulin Level
Description
insulin
Time Frame
Baseline, 12 weeks
Title
Change in C-peptide
Description
C-peptide
Time Frame
Baseline, 12 weeks
Title
Change in C-reactive Protein
Description
C-reactive protein
Time Frame
Baseline, 12 weeks
Title
Change in Tumor Necrosis Factor Alpha
Description
tumor necrosis factor alpha
Time Frame
Baseline, 12 weeks
Title
Change in Interleukin 6
Description
Interleukin 6
Time Frame
Baseline, 12 weeks
Other Pre-specified Outcome Measures:
Title
Compliance to Whey Protein Consumption as Measured by Percent of the Total Number of Sessions Whey Could Have Been Taken
Description
Medication adherence, visual analog scale
Time Frame
Baseline, 12 weeks post study
Title
Change in Food Craving Acceptance and Action Questionnaire Score
Description
The Food Craving Acceptance and Action Questionnaire is a 10-item questionnaire which measures acceptance of food related cravings and urges using a Likert scale (1-7 point scale: never true = 1 to always true = 7). Total scores range 10-70: higher scores indicate greater acceptance of food related cravings and urges.
Time Frame
Change score from pre/post (baseline - at end of initial MOWI 12 weeks; follow-up at end of Maintenance study 6 months post-end of MOWI)
Title
Change in Discomfort Intolerance Scale Score
Description
The Discomfort intolerance Scale is a 6-item questionnaire which measures general difficulty managing and regulating physical distress and discomfort using a Likert scale (1-6 point scale: not at all like me = 1 to very much like me = 6). Total scores range 6-36: higher scores indicate greater distress intolerance.
Time Frame
Change score from pre/post (baseline - at end of initial MOWI 12 weeks; follow-up at end of Maintenance study 6 months post-end of MOWI)
Title
Change in Physical Activity Acceptance & Action Questionnaire Score
Description
The Physical Activity Acceptance & Action Questionnaire is a 10-item scale which measures acceptance of physical and psychological discomfort in the context of physical activity using a Likert scale (1-7 point scale: never true = 1 to always true = 7). Total scores range 10-70: higher scores indicate greater acceptance of physical and psychological discomfort in the context of physical activity.
Time Frame
Change score from pre/post (baseline - at end of initial MOWI 12 weeks; follow-up at end of Maintenance study 6 months post-end of MOWI)
Title
Change in Weight Control Strategies Scale Score
Description
The Weight Control Strategies Scale is a 30-item questionnaire which measures participants' use of behavioral weight control strategies using a Likert scale (1-4 point scale: never = 0 to always = 4). Total scores range 0-120: higher scores indicate greater use of weight control strategies.
Time Frame
Change score from pre/post (baseline - at end of initial MOWI 12 weeks; follow-up at end of Maintenance study 6 months post-end of MOWI)
Title
Change in Voluntary Exercise Questionnaire Score
Description
The Voluntary Exercise Questionnaire is a brief 6-item questionnaire which measures participants' participation in aerobic and strength training activities over the past 3 months and past week. Two items use a Likert scale (1-7 point scale: never = 1 to 7 = very often) and four items ask participants to report frequency of exercise: 0 = 0 days per week to 7 = 7 days per week). Total score range 2-42: Higher scores indicate greater levels of aerobic and strength training activity.
Time Frame
Change score from pre/post (baseline - at end of initial MOWI 12 weeks; follow-up at end of Maintenance study 6 months post-end of MOWI)
Title
Change in Behavioural Regulation in Exercise Questionnaire (BREQ-3) Score
Description
a 24-item assessment of external, introjected, identified, and intrinsic forms of regulation of exercise behavior. Higher scores indicated higher exercise behavior. each is scored on 5 points (0-120). Six subscales - each 4 items (score 0-20 each). A positive change score indicates higher forms of regulation.
Time Frame
Change score from pre/post (baseline - at end of initial MOWI 12 weeks; follow-up at end of Maintenance study 6 months post-end of MOWI)
Title
Change in PROMIS Emotional Distress Short Form Score
Description
an 8 item scale used to measure emotional distress/depression. higher score indicates higher distress. All promis questionnaires raw scores are converted to a scaled score of 0-100. 50 is mean. 10 units on the scale indicate 1 Standard deviation. higher change scores represent reduced emotional distress.
Time Frame
Change score from pre/post (baseline - at end of initial MOWI 12 weeks; follow-up at end of Maintenance study 6 months post-end of MOWI)
Title
Change in PROMIS Social Isolation Short Form Score
Description
An 8-item scale used to measure perceived social isolation.higher scores indicate higher isolation. All promis questionnaires raw scores are converted to a scaled score of 0-100. 50 is mean. 10 units on the scale indicate 1 Standard deviation. higher change scores represent high isolation.
Time Frame
Change score from pre/post (baseline - at end of initial MOWI 12 weeks; follow-up at end of Maintenance study 6 months post-end of MOWI)
Title
Change in Three Factor Eating Questionnaire Score
Description
18-item scale measuring eating behavior with 3 subscales (cognitive restraint, emotional eating, uncontrolled eating) using Likert scale (1-4 point scale). Items 1-16 on this scale are reverse scored. The scale score is then entered into the following formula: (cognitive restraint scale score - 3)/9. The outcome is then multiplied by 100. Higher scores indicate higher restraint, emotional eating or uncontrolled eating, respectively. Subscales aretransformed to 0-100 score To calculate the emotional eating sub scale, reverse scored items 2, 4, 7, 10, 14 and 16 are summed and then averaged to generate a mean score. The mean score is then multiplied by 6 to generate a scale score. The scale score is then entered into the following formula: (emotional eating scale score - 6)/18. The outcome is then multiplied by 100. Positive change scores represent lower restraint, higher emotional eating or higher uncontrolled eating.
Time Frame
Change score from pre/post (baseline - at end of initial MOWI 12 weeks; follow-up at end of Maintenance study 6 months post-end of MOWI)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: All Aims: Age ≥65 years Body Mass Index (BMI) ≥ 30kg/m^2 Waist circumference ≥88cm in females or ≥102cm in males Aims 2 & 3: Have Wi-Fi high speed internet Able to obtain medical clearance from doctor Have less than a 5% weight loss in past 6 months No advanced co-morbidity No exercise restrictions Not involved in other research studies that may interfere with participation Exclusion Criteria: Severe mental or life-threatening illness Dementia Substance use History of bariatric surgery Suicidal ideation Unable to perform measures Reside in nursing home No advanced co-morbidity No exercise restrictions Not involved in other research studies that may interfere with participation Aim 4 - had to have completed Aims 2 or 3
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
John A Batsis, MD
Organizational Affiliation
Dartmouth-Hitchcock Medical Center / Dartmouth Medical School
Official's Role
Principal Investigator
Facility Information:
Facility Name
Dartmouth-Hitchcock Medical Center
City
Lebanon
State/Province
New Hampshire
ZIP/Postal Code
03766
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
33653394
Citation
Petersen CL, Christensen BC, Batsis JA. Weight management intervention identifies association of decreased DNA methylation age with improved functional age measures in older adults with obesity. Clin Epigenetics. 2021 Mar 2;13(1):46. doi: 10.1186/s13148-021-01031-7.
Results Reference
derived
Links:
URL
https://clinicaltrials.gov/show/NCT03041831
Description
Mobile Health Obesity Wellness Intervention in Rural Older Adults (MOWI): Qualitative Assessment
URL
https://clinicaltrials.gov/show/NCT03085589
Description
Mobile Health Obesity Wellness Intervention in Rural Older Adults (MOWI): Amulet Technology Development & Validation
URL
https://clinicaltrials.gov/show/NCT03104205
Description
Mobile Health Obesity Wellness Intervention in Rural Older Adults (MOWI): Home-Based Pilot

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