Linking Churches With Parks to Increase Physical Activity Among Latinos
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The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details. |
ClinicalTrials.gov Identifier: NCT03858868 |
Recruitment Status :
Recruiting
First Posted : March 1, 2019
Last Update Posted : October 6, 2020
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Condition or disease | Intervention/treatment | Phase |
---|---|---|
Physical Activity | Behavioral: Church and park-based intervention Behavioral: Standard health education on physical activity | Not Applicable |
Study Type : | Interventional (Clinical Trial) |
Estimated Enrollment : | 1204 participants |
Allocation: | Randomized |
Intervention Model: | Parallel Assignment |
Masking: | None (Open Label) |
Primary Purpose: | Prevention |
Official Title: | Linking Churches With Parks to Increase Physical Activity Among Latinos |
Actual Study Start Date : | March 3, 2019 |
Estimated Primary Completion Date : | April 30, 2022 |
Estimated Study Completion Date : | April 30, 2023 |

Arm | Intervention/treatment |
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Experimental: Church and park-based intervention
Participants at intervention churches will be offered: texting intervention (messages about physical activity); peer leader training; walking groups; park-based fitness classes; sermons; participation in park advisory board; community advocacy.
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Behavioral: Church and park-based intervention
Multiple components involving motivational messages and concrete opportunities for physical activity at the church and the local park. |
Publicly available physical activity materials
Participants at control churches will be offered standard health educational materials (brochures, tip sheets, posters) about physical activity.
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Behavioral: Standard health education on physical activity
Participants will receive publicly available brochures, tip sheets, etc. about physical activity |
- Change in objectively measured physical activity [ Time Frame: Change in physical activity between baseline and 12 months ]Accelerometer-assessed moderate to vigorous physical activity at 12 months as compared to baseline
- Change in fitness level [ Time Frame: Change in fitness level between baseline and 12 months ]Heart rate / fitness as measured by the 3 minute submaximal step test
- Change in waist circumference [ Time Frame: Change in waist circumference between baseline and 12 months ]Objectively measured waist circumference

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Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
- Does not currently meet physical activity guidelines (150 minutes per week)
- Regularly attends study church
- Does not have health condition that would preclude physical activity
Exclusion Criteria:
- Regularly engages in 150 minutes or more of moderate to vigorous physical activity
- Does not regularly attend study church
- Has health condition that would preclude physical activity

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): NCT03858868
Contact: Kathryn P Derose, PhD, MPH | 310-393-0411 ext 6302 | derose@rand.org |
United States, California | |
RAND Corporation | Recruiting |
Santa Monica, California, United States, 90401 | |
Contact: Kathryn P Derose, PhD, MPH 310-393-0411 ext 6302 derose@rand.org |
Principal Investigator: | Kathryn P Derose, PhD, MPH | RAND |
Responsible Party: | Kathryn Derose, Senior Policy Researcher, RAND |
ClinicalTrials.gov Identifier: | NCT03858868 |
Other Study ID Numbers: |
R01CA218188 ( U.S. NIH Grant/Contract ) |
First Posted: | March 1, 2019 Key Record Dates |
Last Update Posted: | October 6, 2020 |
Last Verified: | October 2020 |
Individual Participant Data (IPD) Sharing Statement: | |
Plan to Share IPD: | Yes |
Plan Description: | The final dataset will include self-reported and biometric variables at baseline, 6m and 12m. These will be made available in the form of an electronic database for researchers who successfully complete a registration process. Data will be de-identified and will not contain any direct or indirect identifiers. We will provide a codebook and users must agree to the conditions of use, including restrictions against attempting to identify study participants, destruction of the data after analyses are completed, reporting responsibilities, restrictions on redistribution of the data to third parties, and proper acknowledgement of the data resource. Users must submit brief proposals regarding intended use of the data; the study team will determine the scientific soundness of the proposal, as well as whether adequate data protections in place, as part of the decision for the researcher to be able to access the public use dataset. |
Time Frame: | 6 months after completion of final manuscripts. |
Studies a U.S. FDA-regulated Drug Product: | No |
Studies a U.S. FDA-regulated Device Product: | No |
physical activity community-based health promotion built environment faith-based organizations |