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Trial · NCT03683173

Promoting Physical Activity in Rural Communities

NCT03683173, Not applicable, Completed, Washington University School of Medicine; results first posted 2024-01-08

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Promoting Physical Activity in Rural Communities. Trials, record NCT03683173. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT03683173

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Promoting Physical Activity in Rural Communities
NCT number
NCT03683173
Status
Completed
Phases
Not applicable
Enrollment
1,241 participants, actual
Lead sponsor
Washington University School of Medicine
Conditions
Physical Activity
Interventions
Intervention
First posted
2018-09-25
Last updated
2024-01-08
Results first posted
2024-01-08

Source ClinicalTrials.gov

Registered outcomes2

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryChange in Objective Physical Activity Measured by Accelerometer Measured at Baseline and 18-month Follow-upBaseline and 18-month follow-up
* Participants will wear an accelerometer to measure physical activity. * The outcome measure will measure the weekly minutes of moderate to vigorous physical activity. * Physical activity was measured using the Freedson Adult cutpoint categories from 1998. Each count was measured every 60 seconds/per minute. * Sedentary: 0-99 counts per minute * Light: 100-1951 counts per minute * Moderate: 1952-5724 counts per minute * Vigorous: 5725-9498 counts per minute * Very vigorous: 9499 and up counts per minute
SecondaryNumber of Participants Who Met the Subjective Physical Activity Recommendations as Measured by the Global Physical Activity Questionnaire at Baseline and 18-month Follow-upBaseline and 18-month follow-up.
* Will use the Global Physical Activity Questionnaire to determine the number of participants who met the physical activity recommendations at baseline and at the 18-month follow-up. * The Global Physical Activity Questionnaire measures time spent in vigorous and moderate intensity physical activity in the domains of work, travel, and recreation. Participants will answer yes or no to their involvement in a given intensity (e.g., vigorous or moderate) in a given domain. If the participant answers 'yes' they will be asked on how many days do they partake in the activity, and for how many hours and/or minutes do they partake in the activity. A higher score equates to more physical activity. The range is from 0 minutes per week (no moderate physical activity in a week) to over 150 minutes per week (meeting recommendations) for moderate physical activity, and 0 minutes per week (no vigorous physical activity in a week) to over 75 minutes per week (meeting recommendations).

Outcomes2

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYChange in Objective Physical Activity Measured by Accelerometer Measured at Baseline and 18-month Follow-upBaseline and 18-month follow-upOnly 56 participants (28 enrolled in the Multilevel Intervention Arm and 28 enrolled in the Control Arm) had valid data at baseline and at the 18-month follow-up.minutes per weekMEAN
SECONDARYNumber of Participants Who Met the Subjective Physical Activity Recommendations as Measured by the Global Physical Activity Questionnaire at Baseline and 18-month Follow-upBaseline and 18-month follow-up.The number of participants analyzed includes only those who completed the questionnaire at the indicated time point.ParticipantsCOUNT_OF_PARTICIPANTS

Results by group8

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnits
Change in Objective Physical Activity Measured by Accelerometer Measured at Baseline and 18-month Follow-upMultilevel InterventionBaseline63.46Standard Deviation 84.58minutes per week
Change in Objective Physical Activity Measured by Accelerometer Measured at Baseline and 18-month Follow-upControlBaseline96.94Standard Deviation 85.32minutes per week
Change in Objective Physical Activity Measured by Accelerometer Measured at Baseline and 18-month Follow-upMultilevel Intervention18-month follow-up74.02Standard Deviation 97.63minutes per week
Change in Objective Physical Activity Measured by Accelerometer Measured at Baseline and 18-month Follow-upControl18-month follow-up76.13Standard Deviation 72.79minutes per week
Number of Participants Who Met the Subjective Physical Activity Recommendations as Measured by the Global Physical Activity Questionnaire at Baseline and 18-month Follow-upMultilevel InterventionBaseline292Participants
Number of Participants Who Met the Subjective Physical Activity Recommendations as Measured by the Global Physical Activity Questionnaire at Baseline and 18-month Follow-upControlBaseline287Participants
Number of Participants Who Met the Subjective Physical Activity Recommendations as Measured by the Global Physical Activity Questionnaire at Baseline and 18-month Follow-upMultilevel Intervention18-month follow-up118Participants
Number of Participants Who Met the Subjective Physical Activity Recommendations as Measured by the Global Physical Activity Questionnaire at Baseline and 18-month Follow-upControl18-month follow-up102Participants

Participant flow12

How many started, completed or left each group, period by period.

PeriodMilestoneGroupParticipantsUnits counted
Enrolled and Completed Baseline SurveySTARTEDMultilevel Intervention6277
Enrolled and Completed Baseline SurveySTARTEDControl6147
Enrolled and Completed Baseline SurveyCOMPLETEDMultilevel Intervention6277
Enrolled and Completed Baseline SurveyCOMPLETEDControl6147
Enrolled and Completed Baseline SurveyNOT COMPLETEDMultilevel Intervention00
Enrolled and Completed Baseline SurveyNOT COMPLETEDControl00
Completed Follow-upSTARTEDMultilevel Intervention6277
Completed Follow-upSTARTEDControl6147
Completed Follow-upCOMPLETEDMultilevel Intervention2407
Completed Follow-upCOMPLETEDControl2387

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals6

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityMultilevel Intervention5627
Total, all-cause mortalityControl4614
Total, other adverse eventsMultilevel Intervention0627
Total, other adverse eventsControl0614
Total, serious adverse eventsMultilevel Intervention0627
Total, serious adverse eventsControl0614

Papers4

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
30700262DERIVEDPubMed
35272263DERIVEDPubMed
36268648DERIVEDPubMed
40951381DERIVEDPubMed

Grants1

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

ProjectTitlePrincipal investigatorsOrganizationFunderFiscal years
R01CA211323Multilevel Approaches for Promoting Physical Activity in Rural CommunitiesBROWNSON, ROSS CWASHINGTON UNIVERSITYNATIONAL CANCER INSTITUTE2017 to 2021

Trial comparisons2

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

ComparisonSource
Multilevel Intervention vs Control: deaths from any causeTrial comparisons
Multilevel Intervention vs Control: serious adverse eventsTrial comparisons

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT03683173

GET https://conductscience.org/api/trials/v1/NCT03683173/registered