Clinical trial Recruiting at 1 site Interventional Ages 18 and up

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 typeInterventional
Ages18 Years and up
SexAll
Enrollment50 (estimated)
SponsorUniversity of Pennsylvania
Academic / other
Locations1 site (Philadelphia, Pennsylvania)
StatusRecruiting
StartedJanuary 15, 2026
Main results expectedDecember 30, 2026
Study endsDecember 30, 2026
Registry record updatedFebruary 27, 2026
Trial IDNCT07316478 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

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.

    Recruiting Washington University School of Medicine · St Louis, Missouri · NCT07776444

  • 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.

    Recruiting Centre for Infectious Disease Research in Zambia · Lusaka, Lusaka Province · NCT07753681

  • 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.

    Recruiting St. Jude Children's Research Hospital · Nhamatanda, Sofala · NCT07719972

  • 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.

    Recruiting Phase 1/2 Children's Hospital Medical Center, Cincinnati · Kampala · NCT07708714

  • 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.

    Recruiting Phase 1 Boston Children's Hospital · Boston, Massachusetts · NCT07708350

  • 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.

    Recruiting University of Maryland, Baltimore · Baltimore, Maryland · NCT07674277

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.