A Culturally Adapted, Social Support-Based, Physical Activity Interventions for South Asian Indian Women in the United States
- Conditions
- Sedentary Behavior
- Interventions
- Behavioral: Dyad-based Zoom health coachingBehavioral: Fitbit activity monitorOther: Electronic newsletters
- Registration Number
- NCT05966506
- Brief Summary
The purpose of this study is to assess the feasibility and acceptability of a peer-based dyadic social support health coaching physical activity (PA) intervention in inactive South Asian Indian (SAI) and to explore preliminary effects of the intervention on intermediate outcomes: self-reported and objective moderate-to-vigorous physical activity (MVPA), social support, and self-efficacy .
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- Female
- Target Recruitment
- 20
- inactive SAI (Physical activity (PA) <150 minutes/week)
- physically able to engage in moderate PA
- speak and read English; able to enroll with an eligible adult female partner who does not live in the same household
- willing to use the Fitbit app/device
- own a smartphone that is compatible with Fitbit software (up to 223.3 MB on iPhone or 165 MB on Android) 9)
- able and willing to send and receive text messages
- Blood pressure reading <160/100 mm Hg, or with medical clearance.
- SAI women with a current/planned pregnancy
- cannot speak and read English
- those participating in a PA or weight loss program
- those diagnosed with a physical disability that interferes with their ability to be physically active.
- not living in Houston, Texas
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Health coaching Dyad-based Zoom health coaching - Health coaching Fitbit activity monitor - Health coaching Electronic newsletters -
- Primary Outcome Measures
Name Time Method Feasibility as assessed by the percentage of participants enrolled in the study 12 weeks Feasibility as assessed by the percentage of participants who complete the study 12 weeks Feasibility as assessed by the number of participants who adhere to treatment 12 weeks Treatment adherence will be calculated as the proportion of intervention sessions attended.
Feasibility as assessed by the number of participants who complete all the assessments 12 weeks Assessments include counseling calls ,use of Fitbit, receipt and review of newsletters
- Secondary Outcome Measures
Name Time Method Change in physical activity as assessed by the Godin Leisure-Time Exercise Questionnaire Baseline, 12 weeks This is a self reported questionnaire with 3 questions. A score of 24 units or more indicates participant is active and score of less than 14 units show participant is insufficiently active or sedentary.
Change in physical activity as assessed by the values on a fitbit Baseline, 12 weeks Change in self-efficacy for PA as assessed by the Self-efficacy for physical activity (SEPA) scale Baseline, 12 weeks This is a five item questionnaire and is scored on a five point Likert-scale, ranging from not confident to extremely confident.
Cognitive impairment as measured by the Montreal Cognitive Assessment (MoCA) 12 weeks Total score on the Montreal Cognitive Assessment (MoCA) range from 0 to 30, with a higher score indicating a better outcome.
Change in PA-related social support as assessed by the Social Support for Physical Activity Survey Baseline, 12 weeks This is a 26 item questionnaire and each is scored from 1(one) to 6(very often) a higher number indicating more social support
Change in PA-related autonomy support as assessed by the Climate Questionnaire (autonomy support) Baseline, 12 weeks This is a 12 item questionnaire (first 6 about partner and the next 6 about participant ) Response options are on a 7-point scale (1=not at all true, 4=somewhat true, 7=very true)
Trial Locations
- Locations (1)
The University of Texas Health Science Center at Houston
🇺🇸Houston, Texas, United States