Can a phone app tame sickle cell pain and cut opioid use?
NCT ID NCT04484272
First seen Aug 21, 2026 · Last updated Sep 02, 2026 · Updated 2 times
Summary
This trial tests whether a smartphone app called You Cope, We Support (YCWS) can help adults with sickle cell disease better manage stress and pain, and possibly reduce opioid use. Participants will be randomly assigned to either use the app along with self-monitoring, or just self-monitor their symptoms. The study will compare changes in pain intensity, stress levels, and opioid use over eight weeks and six months.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- A smartphone app called You Cope, We Support (YCWS) that provides relaxation and distraction exercises, plus self-monitoring of pain, stress, and opioid use with alerts and reminders.
- What this could lead to
- If effective, this app could offer a practical, non-drug way to help adults with sickle cell disease reduce stress and pain, and potentially lower their reliance on opioids.
- What could go wrong
- This is a relatively small trial, and the app's benefits may vary. It relies on daily self-reporting, which can be burdensome, and the long-term impact on opioid use is uncertain.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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239 people
The number who actually took part.
- Started
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Apr 2021
- Finished
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Mar 2026
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 99 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * with diagnosis of SCD (e.g., HbSS, HbSC, HbS-beta-0 thalassemia, and HbS-beta+ thalassemia); (b) reports moderate to severe level of pain (\>3 on 0-10 scale) related to SCD within previous 24 hours; (c) uses opioid analgesics on "as needed" or "continuous" basis (d) who speaks and reads English; and (e) is 18 years of age or older Exclusion Criteria: * are legally blind; (b) physically unable to complete procedures; (c) previously participated in our relaxation/distraction intervention feasibility study
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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University of Florida
Gainesville, Florida, 32610, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Can an antioxidant supplement calm sickle cell blood cells?