Sleep and Pain in Sickle Cell Disease
NCT03150433 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 57
Last updated 2025-01-24
Summary
This is a study testing the effects of behavioral sleep interventions on pain and brain function in sickle cell disease.
Conditions
- Sickle Cell Disease
- Sleep Disturbance
- Pain
Interventions
- BEHAVIORAL
-
Behavioral symptom management
Individual sessions focused on behavioral and cognitive strategies for managing sleep disturbance, pain, and other symptoms of sickle cell disease
- OTHER
-
Sickle cell disease management
Individual sessions focused on understanding and managing sickle cell disease
Sponsors & Collaborators
-
University of Maryland
collaborator OTHER -
National Heart, Lung, and Blood Institute (NHLBI)
collaborator NIH - lead OTHER
Principal Investigators
-
Claudia Campbell, PhD · Johns Hopkins University
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- SINGLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Max Age
- 100 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2017-11-05
- Primary Completion
- 2023-06-30
- Completion
- 2023-10-27
Countries
- United States
Study Locations
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