Mindfulness and stress-management program for adults with sickle cell disease
Official title: RCT of Stress Management and Mindfulness Intervention for Patients With Sickle Cell Disease
Run by University of Pennsylvania · NCT07316478 · Data updated 2026-11-12
This program will try a six-week mindfulness and stress-management course to see if it improves quality of life for adults with sickle cell disease who live near Philadelphia.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 50 (estimated) |
| Sponsor | University of Pennsylvania Academic / other |
| Locations | 1 site (Philadelphia, Pennsylvania) |
| Status | Recruiting |
| Started | January 15, 2026 |
| Main results expected | December 30, 2026 |
| Study ends | December 30, 2026 |
| Registry record updated | February 27, 2026 |
| Trial ID | NCT07316478 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults (18+) diagnosed with sickle cell disease who live within about 90 minutes of Philadelphia, can attend weekly group sessions in person or by Zoom, and do not have severe depression or active suicidality.
✕Probably not a fit
People with severe depression or current suicidal thoughts are excluded, and individuals who live too far from Philadelphia or cannot attend scheduled sessions are unlikely to participate or benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
After consenting and completing baseline questionnaires, adults with sickle cell disease are randomly assigned to start the six-week program right away or to a waitlist control that begins after six weeks. The intervention consists of six weekly one-hour group sessions delivered in person at the University of Pennsylvania or via Zoom and includes cognitive-behavioral techniques, relaxation exercises, and mindfulness meditation. Symptom and quality-of-life measures are collected at baseline and after the initial six-week period, and the waitlist group completes the same measures before they receive the intervention. Participants with severe depression or active suicidality are excluded and enrollment is limited to those living within about 90 minutes of Philadelphia.
Why it matters
Potential benefit: If successful, the program could reduce stress, improve coping skills, and lead to better quality of life for people with sickle cell disease.
How similar studies have gone: Mindfulness and CBT-based programs have shown promising but mixed benefits for pain, stress, and quality of life in chronic pain populations and some sickle cell studies, so this approach is supported by prior work but not definitively proven for SCD.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * 18 years of age or older. * Diagnosed with sickle cell disease. * Live within 90 minutes of Philadelphia Exclusion Criteria: \- Severe depression or suicidality
Where it's running
-
University of Pennsylvania
Philadelphia, Pennsylvania, United States Recruiting
Study contacts
- Principal investigator: Melissa G Hunt, PhD — University of Pennsylvania
- Study coordinator: Melissa G Hunt, PhD
- Email: mhunt@psych.upenn.edu
- Phone: 610-529-8055
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Cerebrovascular Reactivity Testing with HD-DOT in Sickle Cell Patients
This study tests whether high-density diffuse optical tomography can measure brain blood flow and oxygen use in people with sickle cell disease, to see how these signals relate to stroke risk.
-
Adapting and testing PEN-Plus in Zambian primary care
Aiming to see if the PEN-Plus package can be adapted and used in two Zambian hospitals to better manage chronic diseases like heart disease, diabetes, hypertension, and sickle cell in primary care.
-
Newborn Sickle Cell Screening in Mozambique
We’re testing a three-part plan to help babies in Mozambique get diagnosed early for sickle cell disease and start care quickly.
-
Optimizing Hydroxyurea in Children with Sickle Cell in Africa
This study tests whether raising hydroxyurea to a maximum tolerated dose is safe and beneficial for Ugandan children with sickle cell anemia already taking a fixed daily dose.
-
Hematopoietic stem cell editing to treat sickle cell disease
This study tests whether a patient’s own blood stem cells can be edited to remove the sickle cell triggering gene and then returned to the patient.
-
Virtual reality options to help with VOC pain in adults with SCD
This study tests whether headset-based virtual reality can help reduce pain for adults with sickle cell disease during vaso-occlusive crises treated in an infusion center.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.