RECRUITING

An mHealth Intervention to Improve Outcomes for Women With HIV/AIDS

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The purpose of this study is: 1. To develop a new mobile health (mHealth) system that will send text messages to remind both pregnant and non-pregnant women with HIV to adhere to their treatment plan (like keeping appointments, fillings prescriptions, and taking their medication) and address individual barriers to HIV care (like stigma, medical mistrust and resilience). 2. The intervention will also include patient navigation and motivational interviewing 2\) Investigators also want to see if the mHealth system is feasible, easily accepted and if it will impact patient health in a positive way.

Official Title

A Multi-Lingual, Culturally-Competent Mobile Health Intervention to Reduce Medical Mistrust, Stigma, and Improve Treatment Adherence Among Women Living With HIV/AIDS (WLWH)

Quick Facts

Study Start:2022-05-02
Study Completion:2026-07-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT03738410

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:FEMALE
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Confirmed HIV diagnosis as per the clinic standard
  2. * Female \>= 18 years old at enrollment
  3. * Currently active or recently returned into care or newly enrolled
  4. * With two or more previously scheduled visits (12 months prior to study enrollment
  5. * in the 12 months prior to enrollment:
  6. * missed one or more visits or
  7. * viral load detectable (\>20 mL) or
  8. * not taking prescribed HIV anti-retroviral medications
  1. * men
  2. * women who are cognitively impaired or are not able to consent for themselves
  3. * non-working cell phone
  4. * adolescents \< 18 years old at enrollment

Contacts and Locations

Study Contact

Lunthita M Duthely, Ed.D.
CONTACT
305-243-5800
lduthely@med.miami.edu

Principal Investigator

Lunthita M Duthely, Ed.D.
PRINCIPAL_INVESTIGATOR
University of Miami

Study Locations (Sites)

University of Miami
Miami, Florida, 33136
United States

Collaborators and Investigators

Sponsor: University of Miami

  • Lunthita M Duthely, Ed.D., PRINCIPAL_INVESTIGATOR, University of Miami

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2022-05-02
Study Completion Date2026-07-31

Study Record Updates

Study Start Date2022-05-02
Study Completion Date2026-07-31

Terms related to this study

Keywords Provided by Researchers

  • mHealth
  • mobile applications
  • culturally-competent
  • HIV stigma
  • Resilience

Additional Relevant MeSH Terms

  • HIV/AIDS