Actively Recruiting

Phase Not Applicable
Age: 15Years - 39Years
All Genders
NCT07402811

Mindfulness-Based Intervention for Pain and Sleep in Adolescents and Young Adults With Sickle Cell Disease

Led by University of Illinois at Chicago · Updated on 2026-02-13

20

Participants Needed

1

Research Sites

20 weeks

Total Duration

On this page

Sponsors

U

University of Illinois at Chicago

Lead Sponsor

N

National Institute of Nursing Research (NINR)

Collaborating Sponsor

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

Mindfulness-Based Intervention for Pain and Sleep in Adolescents and Young Adults With Sickle Cell Disease

Who Can Participate

Age: 15Years - 39Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Individuals aged 15-39 years
  • Diagnosed with sickle cell disease
  • Able to speak and understand English
  • Able to complete questionnaires with little or no help from a caregiver
  • Report pain and/or sleep problems based on ASCQ-Me short forms
  • Have internet access on a smartphone, tablet, or computer
Not Eligible

You will not qualify if you...

  • Significant cognitive limitations impairing use or understanding of the mindfulness intervention, as judged by healthcare provider or caregiver
  • Currently receiving a mindfulness-based intervention or have had more than 4 sessions of any mindfulness program in the past 6 months

AI-Screening

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Trial Site Locations

Total: 1 location

1

University of Illinois Chicago

Chicago, Illinois, United States, 60612

Actively Recruiting

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Research Team

D

Dahee Wi, PhD, RN

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

1

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