NCT07402811Completed
Mindfulness-Based Intervention for Pain and Sleep in Adolescents and Young Adults With Sickle Cell Disease
Source: ClinicalTrials.gov · Last updated 27 Aug 2026
Brief summary (registry, in English)
This study examines the feasibility and acceptability of a mindfulness-based mobile intervention designed to support pain and sleep management among adolescents and young adults with sickle cell disease. Chronic pain and sleep problems are common in this population and can negatively affect daily functioning and quality of life. Participants will use a smartphone-based mindfulness program that includes structured modules and guided mindfulness exercises over an approximately 8-week period. The study aims to evaluate whether the intervention is feasible and acceptable for adolescents and young adults with sickle cell disease.
- Status (registry)
- Completed
- Study type
- Interventional
- Enrollment
- 25 (actual)
- First submitted
- 26 Jan 2026
- Start date
- 6 Dec 2025
- Primary completion date
- 8 May 2026
- Lead sponsor
- University of Illinois Chicago
- Diseases
- Sickle cell disease
- NCT number
- NCT07402811
What you commit to
- Study type: Interventional
- Participants enrolled: 25
- From 6 Dec 2025 to the primary completion date, 8 May 2026
- 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
- Are currently receiving an MBI or have received more than 4 sessions of any MBI in the 6 months prior to the screening
Other
- Individuals who have significant cognitive limitations that will impair their ability to use and understand the MBI, as per their health care provider or caregiver
Who the study is looking for
- Individuals aged 15-39 years
- Have been diagnosed with SCD
- Are able to speak and understand English
- Are able to complete questionnaires with minimal or no assistance from a caregiver
- Report pain and/or sleep problems as assessed by the Adult Sickle Cell Quality of Life Measurement Information System (ASCQ-Me) short forms
- Have access to the internet on a smartphone, tablet, or computer
Age in the registry: 15 years to 39 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 |
|---|---|---|---|
| University of Illinois Chicago Coordinator of this site? Confirm its status | Chicago | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.