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Clinical Trials/NCT02850770
NCT02850770
Completed
Not Applicable

Phone Messaging for Physical Activity and Social Support Prompting Among Low-Income Latino Patients: A Randomized Pilot Study

University of Southern California0 sites42 target enrollmentApril 2015

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Physical Activity
Sponsor
University of Southern California
Enrollment
42
Primary Endpoint
Change in average daily steps assessed by pedometers
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

The objective of this study was to investigate the feasibility, perceived usefulness, and potential effectiveness of a short text or voice message intervention to activate 1) physical activity behavior change among low-income, urban, Latino patients in diabetes management and 2) supportive behaviors by family members or close friends.

Detailed Description

Despite the promise of phone-based interventions to effectively support diabetes self-management (DSM), little is known about their impact on the outcomes of highly vulnerable populations such as low-income, inner-city, racial/ethnic minorities. And while phone-based interventions have generally been successful at reaching and engaging adults with diabetes, they have failed to do the same with family members/friends (FF) whom are a promising source of ongoing support for DSM. The objective of this study was to investigate the feasibility, perceived usefulness, and potential effectiveness of a short text or voice message (ST/VM) intervention to activate 1) physical activity (PA) behavior change among low-income, urban, Latino patients in diabetes management and 2) supportive behaviors by FF. The investigators conducted a 12-week pilot study in which participants were randomized into one of three study arms: control, phone messaging (PM), and phone messaging plus social support from FF (PM+FF). Participants were recruited in person from a diabetes management program at a safety-net ambulatory care clinic. All participants were given a pedometer and walking log for self-monitoring. Participants in the PM and PM+FF arms received ST/VMs as reminders to review daily step goals and to self-monitor; explaining the benefits of regular PA, importance of regular PA to daily life, and ways to overcome commonly identified barriers to PA; asking participants to report on PA performance; providing feedback based on responses. Participants in the PM+FF identified a FF to receive ST/VMs with suggested behaviors that are perceived as supportive by individuals making PA behavior changes. Participants received semi-structured assessments in person at baseline, 6 weeks, and 12 weeks. Participants were asked about the extent to which the program enhanced the participant's ability to make PA behavior changes. The primary outcome measures were daily step counts and perceived FF social support.

Registry
clinicaltrials.gov
Start Date
April 2015
End Date
November 2015
Last Updated
9 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Shinyi Wu

Associate Professor

University of Southern California

Eligibility Criteria

Inclusion Criteria

  • Age greater than or equal to 18 years
  • Diagnosis of type 2 diabetes
  • No medical conditions restricting patient from beginning a walking program
  • Preferred language of English or Spanish, self-identifies as a Hispanic
  • Ability to walk without the use of assistive devices such as canes or walkers
  • Available to attend three interviews at the clinic
  • Does not plan to move away from the region or be out of the country during the next three months
  • Has a working phone where they can receive regular short text or voice messages for three months

Exclusion Criteria

  • Pregnant or breastfeeding women

Outcomes

Primary Outcomes

Change in average daily steps assessed by pedometers

Time Frame: Baseline, 6 weeks, 12 weeks

Change in average daily steps assessed using pedometer 7-day data storage

Secondary Outcomes

  • Change in barriers self-efficacy assessed using the Barriers Self-Efficacy Scale(Baseline, 6 weeks, 12 weeks)
  • Change in body mass index(Baseline, 6 weeks, 12 weeks)
  • Change in exercise self-efficacy assessed using the Exercise Self-Efficacy Scale(Baseline, 6 weeks, 12 weeks)
  • Change in perceived family/friend social support assessed using the Social Support and Exercise Survey(Baseline, 6 weeks, 12 weeks)

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