Activity Level Monitoring Study
- Conditions
- Morbid ObesityObesity
- Interventions
- Behavioral: Phone/zoom calls
- Registration Number
- NCT05379088
- Lead Sponsor
- Ohio State University
- Brief Summary
The purpose of this study is to 1) evaluate the relationship of physical activity to quality of life and psychological functioning among adults with severe obesity (BMI\>40) and 2) evaluate the effects of activity monitoring on changes in physical activity during a 6-week intervention interval.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ACTIVE_NOT_RECRUITING
- Sex
- All
- Target Recruitment
- 38
- 18 years of age or older
- BMI greater than or equal to 40
- Sit or lie down greater than or equal to 9 hours per day
- Participating in regular exercise (any planned exercise)
- Participating in a formal weight loss or exercise program
- Planning to join a formal weight loss or exercise program in the next 2 months
- Cannot stand up without assistance
- Currently pregnant
- Planning to get pregnant in the next 2 months
- Given birth in past 9 months
- Currently breast feeding
- Weigh over 400 lbs
- Highest level of education is below 8th grade
- PHQ-9 score less than 15
- Visual impairment that impairs ability to read
- Any condition(s) that would make it challenging to follow instructions/directions
- Cognitive disorder (e.g., dementia)
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Additional Follow-up Phone/zoom calls In addition to receiving an ActiGraph activity monitor, participants will complete weekly phone/zoom calls with research staff for a more in-depth monitoring of their activity level.
- Primary Outcome Measures
Name Time Method Physical function Change from baseline to 6 weeks Participants will complete a 60-foot walk test and 30-second chair stand test.
Sit to stand transitions Change from baseline to 6 weeks Participants will wear activity monitors for the duration of the study. The monitors will keep track of every time a participant goes from sitting to standing and vice versa.
Health Related Quality of life Change from baseline to 6 weeks Participants will complete the Medical Outcomes Survey, Short Form-36
Sedentary time Change from baseline to 6 weeks Participants will wear activity monitors for the duration of the study. Sedentary time is operationalized as any recorded waking time spent sitting or lying down.
Self-report physical activity Change from baseline to 6 weeks Participants will complete the Modified International Physical Activity Questionnaire - Short Form
- Secondary Outcome Measures
Name Time Method Psychological distress Change from baseline to 6 weeks Participants will complete the Hospital and Anxiety Scale
Weight Stigma measure 3 Change from baseline to 6 weeks Participants will complete the Body Appreciation Scale
Pain perception measure 1 Change from baseline to 6 weeks Participants will complete the McGill Pain Questionnaire
Weight Stigma measure 2 Change from baseline to 6 weeks Participants will complete the Weight Bias Internalization Scale
Perceived stress Change from baseline to 6 weeks Participants will complete the Perceived Stress Scale
Pain perception measure 2 Change from baseline to 6 weeks Participants will complete the Visual Analog Scale for Pain
Weight Stigma measure 1 Change from baseline to 6 weeks Participants will complete the Stigma Situations Inventory
Insomnia Change from baseline to 6 weeks Participants will complete the Insomnia Severity Index
Sleep quality Change from baseline to 6 weeks Participants will complete the Pittsburgh Sleep Quality Index
Trial Locations
- Locations (1)
The Ohio State University
🇺🇸Columbus, Ohio, United States