NCT06511453Active, not recruiting
Acupressure in Patients With Sickle Cell Disease
Remote Self-Administered Acupressure for Pain Management in Patients With Sickle Cell Disease
Source: ClinicalTrials.gov · Last updated 31 Jul 2026
Brief summary (registry, in English)
The proposed research is to determine the clinical efficacy and neurobiological mechanisms of acupressure analgesia in patients with sickle cell disease (SCD).
- Status (registry)
- Active, not recruiting
- Study type
- Interventional
- Enrollment
- 59 (actual)
- First submitted
- 10 Jul 2024
- Start date
- 7 Mar 2024
- Primary completion date
- 30 Jan 2026
- Lead sponsor
- Indiana University
- Diseases
- Sickle cell disease
- NCT number
- NCT06511453
What you commit to
- Study type: Interventional
- Participants enrolled: 59
- From 7 Mar 2024 to the primary completion date, 30 Jan 2026
- 2 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Presence of a concurrent autoimmune or inflammatory disease such as rheumatoid arthritis, systemic lupus erythematosus, inflammatory bowel disease, etc. that causes pain or any other chronic pain condition with pain greater than sickle pain.
Other illness
- Diseases/conditions history includes but not limited to:
- Known non-SCD-related severe psychiatric illnesses (e.g. current schizophrenia, major depression with suicidal ideation).
- Significant visual, motor, or auditory impairment that would interfere with ability to perform study visits-related activities
Other
- Recent/ongoing alternative pain management with acupuncture/acupressure or acupuncture/acupressure-related techniques within the last 6 months.
- Head injury with substantial loss of consciousness
Who the study is looking for
- Any gender
- 18-80 (Adults) years old
- Have been diagnosed with SCD and experiencing chronic pain in the past 6 months or vaso-occlusive crisis/crises in the past 12 months.
- Either outpatient or inpatient or status changing between each other
- Willing to limit the current and the introduction of any new medications or treatment modalities for control of pain symptoms during the study visits.
- Willing to stick to the scheduled acupressure treatments every other day for 5 weeks.
- Fluent in English and capable of giving written informed consent.
Age in the registry: 18 years to 80 years · Sex: All · Accepts healthy volunteers
Sites (2)
Sites in registry order. Save your city in your profile to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Indiana University School of Medicine Coordinator of this site? Confirm its status | Indianapolis | United States | Unknown status |
| University of California, Irvine Coordinator of this site? Confirm its status | Irvine | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.