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NCT07875777Not yet recruiting

Self-administered Acupressure in Patients With Sickle Cell Disease

Acupressure in Patients With Sickle Cell Disease

Source: ClinicalTrials.gov · Last updated 15 Oct 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)
Not yet recruiting
Study type
Interventional
Enrollment
300 (estimated)
First submitted
8 Oct 2026
Start date
1 Oct 2027
Primary completion date
30 Sept 2032
Lead sponsor
University of Cincinnati
NCT number
NCT07875777

What you commit to

  • Study type: Interventional
  • Planned participants: 300
  • From 1 Oct 2027 to the primary completion date, 30 Sept 2032
  • 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:
  • Head injury with substantial loss of consciousness 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

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
  • 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 · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
University of Cincinnati
Coordinator of this site? Confirm its status
CincinnatiUnited StatesUnknown status
University of California, Irvine
Coordinator of this site? Confirm its status
IrvineUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.