NCT04023487Completed
Evaluation of an Intervention for Young Adults With Diabetes: Resilient, Empowered, Active Living-Telehealth (REAL-T)
Evaluation of a Complex Intervention for Young Adults With Diabetes: The Resilient, Empowered, Active Living-Telehealth (REAL-T) Study
Source: ClinicalTrials.gov · Last updated 21 Aug 2026
Brief summary (registry, in English)
This study will evaluate (1) the efficacy of REAL-T, a lifestyle-based telehealth intervention, in improving glycemic control (HbA1c) and psychosocial outcomes, (2) which effects are retained over a 6-month follow-up period, and (3) the mediating mechanisms responsible for the intervention's effects. Half of participants will receive REAL-T, while the other half will receive their usual care.
- Status (registry)
- Completed
- Study type
- Interventional
- Enrollment
- 209 (actual)
- First submitted
- 15 Jul 2019
- Start date
- 22 Oct 2019
- Primary completion date
- 5 Jun 2023
- Lead sponsor
- University of Southern California
- Diseases
- Type 1 diabetes
- NCT number
- NCT04023487
What you commit to
- Study type: Interventional
- Participants enrolled: 209
- From 22 Oct 2019 to the primary completion date, 5 Jun 2023
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Previously received REAL intervention
Other illness
- Cognitive impairment or severe disability limiting life expectancy
Other
- Currently pregnant or planning to become pregnant within the next 12 months
Who the study is looking for
- T1D for ≥12 months
- A1c ≥7.5% at time of study enrollment
- Age 18-30 yrs. at time of study enrollment
- English or Spanish speaking
- Resides in a state where OT clinicians are licensed, in an area where the participant has access to a local healthcare provider in the event of emergency and can complete data collection in person (when permitted) or via mailings (when required during period of social distance or due to distance from study site)
- Participant has access to a laptop or desktop computer, either their own or loaned by the study (if geographically feasible and permitted given COVID-19 social distancing distractions)
- Willing to participate in 6-month intervention
Age in the registry: 18 years to 30 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| USC Center for Health Professionals Coordinator of this site? Confirm its status | Los Angeles | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.