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OpenTrials
Completed

NCT Number: NCT02986945

Community-Partnered Participatory Development of Mobile Interventions

The purpose of the study is to test an experimental method, a text-messaging app called B-RESILIENT, for improving participants' mood. B-RESILIENT is a text messaging app adaptation of a Resiliency Course, developed by community members known as Building Resiliency and Community Hope.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Healthy African American Families

Los Angeles, California, 90008, United States

About this study

In phase 1, the investigators held a series of in-person and virtual workshops with the Partnered Research Center for Quality Care (PRC) community partners to co-develop mobile interventions to address community priorities. The goal of the workshops was to develop novel mobile interventions based on stakeholder input. The specific intervention to be developed was determined based on stakeholder input regarding community priorities during the workshops. Workshops were audio and/or video recorded to document the process. One of the tools used in this process was the Chorus Participatory Mobile Framework created at the Center for Health Services and Society at UCLA. Chorus is a web application that allows users to easily create mobile (text messaging and interactive voice) applications in real-time without requiring any server programming. The investigators used this framework during the workshops to develop and test the application in real-time. Participants were also given phone numbers to call or text in to the intervention that they co-developed for the purpose of testing, providing feedback, and guiding future development.

In phase 2, the investigators will conduct a pilot randomized control trial of the B-RESILIENT tool developed during the workgroup phase 1. Investigators will enroll 30 adults in South Los Angeles to participate in a randomized, wait-list trial. The study group will receive the intervention for 4 weeks, followed by the wait-list group for another 4 weeks. Investigators will conduct baseline and follow-up surveys, as well as in-person or telephone workgroups, to assess the tool's usability and feasibility for supporting management of mood and depressive symptoms.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age 18 or older
  • Speak English
  • Endorse one item on the PHQ-2
  • Are able to be contacted by phone or email, and have a cell phone that receives text messages
  • Have internet access

Exclusion criteria

  • Under age 18 years
  • Endorse no items on PHQ-2 screener
  • PHQ-8 score of 15 or greater on the baseline interview
  • No cell phone and internet access
  • Currently homeless
  • Has a prior diagnosis of schizophrenia, psychosis, bipolar disorder
  • Current alcohol and substance abuse

Treatment and study plan

Resiliency App

Behavioral

Other names: B-RESILIENT

Primary outcomes

  1. Depressive symptom count as measured by the Patient Health Questionnaire 8

    Time frame: Change from baseline at 1 month

    The Patient Health Questionnaire (PHQ) 8 is a standard measure of depressive symptoms.

Other outcomes

  1. Fordyce Emotions Questionnaire

    Time frame: Change from baseline at 1 month

    This questionnaire assesses current happiness with four questions. The first question assesses current happiness on a scale of 0 (extremely unhappy) to 10 (extremely happy). Questions 2 through 4 asks the percent of time the respondent feels happy; percent of time unhappy; and percent of time neutral.

  2. Brief Resilience Scale

    Time frame: Change from baseline at 1 month

    A 6 item measure of the ability to bounce back or recover from stress.

  3. Coping Strategies

    Time frame: Change from baseline at 1 month

    The coping strategies questionnaire is a 4 item measure used to determine any use of avoidant and/or active coping strategies to stressful situations or problems.

  4. Social Supports

    Time frame: Change from baseline at 1 month

    The social support survey is a 10 item measure created to help assess various dimensions of social support (emotional, affectionate, and positive social interaction).

  5. Employment, work missed for those employed

    Time frame: Change from baseline at 1 month

    The employment questionnaire has 1 item that assesses the employment situation of participants. There are 4 additional items reporting any days missed of work.

  6. Income

    Time frame: Change from baseline at 1 month

    The income survey is a 1 item measure created to evaluate the level of income within each household.

  7. Client Use of Services

    Time frame: Change from baseline at 1 month

    The client use of services Scale is an 6 item measure that assesses access to and use of general health services in the community. This includes hospitalizations, ER visits, Mental Health Services, Social and Community-based Services, and other trusted locations.

  8. Current Medication Use

    Time frame: Change from baseline at 1 month

    The current medication use is a measure with 2 items created to identify any prescribed medications being consumed for mental or emotional problems such as depression, anxiety, or nerves.

Sponsors and collaborators

Lead sponsor

RAND

Other

Collaborators

  • University of California, Los Angeles

Registry information

Important dates

Study start
2016
Primary completion
2017
Study completion
2017
First posted
Dec 8, 2016
Registry last updated
Apr 17, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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