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South Asians Active Together (SAATH) Study

A Multilevel Physical Activity Intervention for South Asian Women and Girls (SAATH)

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04400253
Enrollment
252
Registered
2020-05-22
Start date
2020-08-01
Completion date
2024-03-26
Last updated
2024-11-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Physical Inactivity, South Asian

Brief 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.

Interventions

BEHAVIORALSAATH Intervention

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

Sponsors

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

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Investigator)

Eligibility

Sex/Gender
FEMALE
Age
11 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

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.

Design outcomes

Primary

MeasureTime frameDescription
Averaged daily minutes spent in moderate- and vigorous-intensity physical activity measured by ActiGraph accelerometersThe outcome will be assessed before the intervention (week 0) and after the intervention (week 18)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

Secondary

MeasureTime frameDescription
Averaged daily minutes spent in walking or running behavior measured by ActiGraph accelerometersThe outcome will be assessed before the intervention (week 0) and after the intervention (week 18)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
Averaged daily hours spent in sedentary behaviors measured by ActiGraph accelerometersThe outcome will be assessed before the intervention (week 0) and after the intervention (week 18)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
Systolic and diastolic blood pressure (mmHg) measured by a sphygmomanometerThe outcome will be assessed before the intervention (week 0) and after the intervention (week 18)Blood pressure will be measured three times while sitting down and relaxing on a chair and the last two measures will be averaged
Self-efficacy score measured by the Exercise Confidence SurveyThe outcome will be assessed before the intervention (week 0) and after the intervention (week 18)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
Self-efficacy score measured by Dishman's Barriers to Self-Efficacy questionnaireThe outcome will be assessed before the intervention (week 0) and after the intervention (week 18)The self-efficacy score will be calculated by averaging the responses (scored 1 to 5 point; higher scores mean higher self-efficacy \[a better outcome\])

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026