MOWI Qualitative Assessment
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ClinicalTrials.gov Identifier: NCT03041831 |
Recruitment Status :
Completed
First Posted : February 3, 2017
Last Update Posted : April 29, 2020
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Condition or disease |
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Obesity |
Study Type : | Observational |
Actual Enrollment : | 40 participants |
Observational Model: | Other |
Time Perspective: | Cross-Sectional |
Official Title: | Mobile Health Obesity Wellness Intervention in Rural Older Adults (MOWI): Qualitative Assessment |
Actual Study Start Date : | August 15, 2016 |
Actual Primary Completion Date : | April 28, 2017 |
Actual Study Completion Date : | April 28, 2020 |
Group/Cohort |
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Older adult individual interviews
The investigators will conduct 8 semi-structured 60-minute interviews with patient participants.The goal of these interviews is to determine the acceptability, utility, and perceived value of mobile health (mHealth) in helping older adults overcome barriers to health behavior change.
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Clinician individual interviews
The investigators will conduct 6 semi-structured 60-minute interviews with primary care clinicians who care for older adult populations.The goal of these interviews is to determine the acceptability, utility, and perceived value of mobile health (mHealth) in helping older adults overcome barriers to health behavior change.
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Community leader individual interviews
The investigators will conduct 4 semi-structured 60-minute interviews with community leaders.The goal of these interviews is to determine the acceptability, utility, and perceived value of mobile health (mHealth) in helping older adults overcome barriers to health behavior change.
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Focus group discussions
The investigators will lead four 90-minute focus group discussions consisting of 6-8 older adult participants each. The goal of these focus groups is to determine the acceptability, utility, and perceived value of mobile health (mHealth) in helping older adults overcome barriers to health behavior change.
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- Technology use in older adults [ Time Frame: Up to one year from interview or focus group ]The investigators will record and transcribe each interview and focus group discussion for post-hoc evaluation. The investigators will then use the transcripts to identify themes on perceptions and experience with technology use in older adults.
- Determinants of obesity in older adults [ Time Frame: Up to one year from interview or focus group ]The investigators will record and transcribe each interview and focus group discussion for post-hoc evaluation. The investigators will then use the transcripts to identify themes related to the secondary outcome. Themes may include (but are not limited to) barriers and facilitators experienced by older adults when they want to lose weight or eat healthier, barriers and facilitators to joining wellness programs, and general availability of options and support.

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Ages Eligible for Study: | 65 Years and older (Older Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | Yes |
Sampling Method: | Non-Probability Sample |
Inclusion Criteria:
- Age ≥65 years;
- Body Mass Index (BMI) ≥ 30kg/m^2;
- Waist circumference ≥88cm in females or ≥102cm in males
Exclusion Criteria:
- Severe mental or life-threatening illness
- Dementia
- Substance use
- History of bariatric surgery
- Suicidal ideation
- Unable to perform measures
- Reside in a nursing home

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03041831
United States, New Hampshire | |
Dartmouth-Hitchcock Medical Center | |
Lebanon, New Hampshire, United States, 03766 |
Principal Investigator: | John A Batsis, MD | Dartmouth-Hitchcock Medical Center / Dartmouth Medical School |
Documents provided by John A. Batsis, MD, Dartmouth-Hitchcock Medical Center:
Publications of Results:
Responsible Party: | John A. Batsis, MD, Associate Professor of Medicine and of The Dartmouth Institute Geisel School of Medicine at Dartmouth, Dartmouth-Hitchcock Medical Center |
ClinicalTrials.gov Identifier: | NCT03041831 |
Other Study ID Numbers: |
D16182_1a K23AG051681 ( U.S. NIH Grant/Contract ) |
First Posted: | February 3, 2017 Key Record Dates |
Last Update Posted: | April 29, 2020 |
Last Verified: | April 2020 |
Individual Participant Data (IPD) Sharing Statement: | |
Plan to Share IPD: | No |
frail elderly telemedicine obesity rural health health promotion |
Obesity Overnutrition Nutrition Disorders Overweight Body Weight |