Promotora-Led Physical Activity Intervention Trial for Latinas in Texas

NCT02046343 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 712

Last updated 2018-08-31

No results posted yet for this study

Summary

The purpose of this study it to determine if a promotora-led intervention that takes a comprehensive, multi-level, community-based approach to promoting physical activity (PA) is effective among a particularly underserved segment of Latinas. We hypothesize that Latinas in the promotora-led PA Intervention will significantly increase minutes per week of moderate-to-vigorous physical activity (MVPA) compared to Latinas in the attention-control group.

Conditions

  • Physical Activity

Interventions

BEHAVIORAL

Health education

Group health education sessions delivered by a promotora approximately 90 minutes in length. In the PA arm, health education incorporates at least 30 minutes group exercise.

BEHAVIORAL

Telephone Counseling

Brief (10 minute) telephone counseling calls delivered by promotoras using motivational interviewing techniques. The counseling calls will emphasize behavior change strategies, including self-monitoring, goal setting, reinforcement, problem solving, stimulus control, and enlisting social support.

OTHER

Newsletter

Educational, motivational and informational newsletters tailored for each community and hand-delivered by promotoras to participant homes.

OTHER

Environmental Change

Create a site atmosphere that promotes PA and increases the number of PA program offerings.

Sponsors & Collaborators

  • National Heart, Lung, and Blood Institute (NHLBI)

    collaborator NIH
  • University of South Carolina

    collaborator OTHER
  • The University of Texas Health Science Center, Houston

    collaborator OTHER
  • Texas A&M University

    collaborator OTHER
  • Texas Tech University Health Sciences Center, El Paso

    collaborator OTHER
  • University of Maryland

    collaborator OTHER
  • The University of Texas Health Science Center at San Antonio

    lead OTHER

Principal Investigators

  • Deborah M Parra-Medina, PhD · UT Health San Antonio

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
64 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2012-08-31
Primary Completion
2016-12-31
Completion
2016-12-31

Countries

  • United States

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02046343 on ClinicalTrials.gov