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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04400253
Other study ID # STU00211374:
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date August 1, 2020
Est. completion date July 31, 2024

Study information

Verified date October 2023
Source Northwestern University
Contact Namratha Kandula, MD, MPH
Phone +1 312 503 6470
Email n-kandula@northwestern.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

South Asian immigrant women and girls are at increased risk for insufficient physical activity and are not being reached by current approaches to physical activity promotion. This randomized control trial study will test the effectiveness and implementation of a multi component physical activity intervention directed at the environment, family, interpersonal and individual levels to promote physical activity among South Asian immigrant mothers and daughters.


Recruitment information / eligibility

Status Recruiting
Enrollment 320
Est. completion date July 31, 2024
Est. primary completion date July 31, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 11 Years and older
Eligibility The sample of this study is South Asian mothers and their daughters. The inclusion criteria for the mother include: - Identifying herself as South Asian, - having a sedentary lifestyle as assessed using a self-report questionnaire - having ability to communicate in Hindi, Gujarati, Urdu, or English. - Having a daughter aged 11-16 years Exclusion Criteria: - having known medical condition that restricts ability to participate in moderate intensity Physical Activity - Unable to complete study procedures (including not wearing accelerometer during run-in) - Currently pregnant - Unable to provide informed consent or assent.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
SAATH Intervention
SAATH intervention is a physical activity intervention for South Asian mothers and daughters with group exercise classes and discussion groups.

Locations

Country Name City State
United States Northwestern University-Feinberg School of Medicine Chicago Illinois

Sponsors (7)

Lead Sponsor Collaborator
Northwestern University Ann & Robert H Lurie Children's Hospital of Chicago, Metropolitan Asian Family Services, Skokie Health Department, Skokie Park District, University of Chicago, University of Illinois at Chicago

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Averaged daily minutes spent in moderate- and vigorous-intensity physical activity measured by ActiGraph accelerometers Moderate- and vigorous-intensity physical activity will be identified based on the accelerometer count cut-point for moderate intensity and daily minutes spent in moderate- and vigorous-intensity physical activity estimated for seven days will be averaged The outcome will be assessed before the intervention (week 0) and after the intervention (week 18)
Secondary Averaged daily minutes spent in walking or running behavior measured by ActiGraph accelerometers Walking and running behavior will be recognized using a machine learning activity recognition algorithm and daily minutes spent in walking or running behavior estimated for seven days will be averaged The outcome will be assessed before the intervention (week 0) and after the intervention (week 18)
Secondary Averaged daily hours spent in sedentary behaviors measured by ActiGraph accelerometers Sedentary behaviors will be identified based on the accelerometer count cut-point for sedentary behaviors and daily minutes spent in sedentary behaviors estimated for seven days will be averaged The outcome will be assessed before the intervention (week 0) and after the intervention (week 18)
Secondary Systolic and diastolic blood pressure (mmHg) measured by a sphygmomanometer Blood pressure will be measured three times while sitting down and relaxing on a chair and the last two measures will be averaged The outcome will be assessed before the intervention (week 0) and after the intervention (week 18)
Secondary Self-efficacy score measured by the Exercise Confidence Survey The self-efficacy score will be calculated by averaging the responses (scored 1 to 5 point for the responses of strongly disagree to strongly agree) from each question item The outcome will be assessed before the intervention (week 0) and after the intervention (week 18)
Secondary Self-efficacy score measured by Dishman's Barriers to Self-Efficacy questionnaire The self-efficacy score will be calculated by averaging the responses (scored 1 to 5 point; higher scores mean higher self-efficacy [a better outcome]) The outcome will be assessed before the intervention (week 0) and after the intervention (week 18)
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