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Study identifier: NCT04484272 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

A Stress and Pain Self-management m-Health App for Adult Outpatients With Sickle Cell Disease

Condition: Sickle Cell Disease  ·  Sponsor: University of Florida

PhaseNA
Planned participants185
Who can joinAll sexes, 18 Years to 99 Years
Healthy volunteersNo

About this study

Our long-term goal is to reduce stress and improve sickle cell disease (SCD) pain control with less opioid use through an intervention with self-management relaxation/distraction exercises (RDE), named You Cope, We Support (YCWS). Americans living with SCD suffer recurrent episodes of acute and chronic pain, both of which are exacerbated by stress. Building on the successes of our prior formative studies, we now propose a well-designed, appropriately powered study to test efficacy of YCWS on outcomes (pain intensity, stress intensity, opioid use) in adults with SCD. We propose to recruit 170 adults for a randomized controlled trial of the short-term (8 weeks) and long-term (6 months) effects of YCWS on outcomes (pain, stress, and opioid use). Stratified on worst pain intensity (\<=5; \>5), we will randomly assign patients to groups: 85 to Control (Self-monitoring of outcomes + alerts/reminders), and 85 to Experimental (Self-monitoring of outcomes + alerts/reminders + use of YCWS \[RDE + Support\]). We will ask participants to report outcomes daily. During weeks 1-8, we will send system-generated alerts/reminders to both groups via phone call, text, or email to facilitate data entry (both groups) and intervention use support (experimental). If the patient does not enter data after 24 hours, study support staff will contact him/her for data entry trouble-shooting (both groups) and YCWS use (experimental). We will time stamp and track participants' online activities to understan…

This description comes directly from the study's public registry record.

Talk to the study team

Muntaha Ali, MS  ·  352-273-6520  ·  muntahaali@ufl.edu

Amelia Greenlee  ·  352-273-6356  ·  greenleeal@ufl.edu

Always discuss trial participation with your own doctor first.

Locations (1)

University of FloridaGainesville, Florida, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT04484272