Actively Recruiting
Exploratory Study on Global Reflexology in Sickle Cell Disease
Led by Hospices Civils de Lyon · Updated on 2025-07-08
30
Participants Needed
1
Research Sites
108 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Sickle cell disease (or sickle cell anemia) is the most common genetic disease in France with 586 children screened in 2019. This chronic disease is characterized by the presence of abnormal Hemoglobin (Hb) S and a deformation of the red blood cells which take the elongated shape of a sickle and become more rigid and more fragile. Sickle cell disease manifests itself among other things by very painful vaso-occlusive crises (VOC) and for some chronic pain. Their management is an emergency and often requires hospitalization. Despite analgesic treatment, some patients have persistent pain. In 2013, a childcare assistant trained in Canadian global reflexology EMC offered reflexology sessions to 12 sickle cell patients. She observed a relief in all patients with a decrease in the pain score in 8 of them. These sessions seem to show us a double interest: the reduction of the child\'s pain and the emergence of a technique that can be used by paramedics in the context of their own role. The investgators hypothesize that global reflexology is an effective and acceptable complementary technique for pain management in addition to the usual analgesic management in sickle cell children under 18 years of age in CVO. In order to verify our hypothesis, the investigators propose to explore the practice of Canadian global reflexology as an innovative therapeutic option complementary to drug treatments in the hospital management of sickle cell children.
CONDITIONS
Official Title
Exploratory Study on Global Reflexology in Sickle Cell Disease
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patient under 18 years of age
- Patient suffering from sickle cell disease
- Patient hospitalized in the UHCD or USC unit of the Women's Mother and Child Hospital of the Hospices Civils de Lyon for the management of a vaso-occlusive crisis
- Informed consent signed by at least one holder of parental authority
- Collection of the patient's assent as soon as age allows it
You will not qualify if you...
- Patient receiving patient-controlled analgesia (PCA)
- Patient receiving nurse-controlled analgesia (NCA)
- Patient not affiliated with a social security scheme or similar beneficiary
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Hôpital Femme Mère Enfant
Bron, France, 69500
Actively Recruiting
Research Team
C
COLLOT Sophie
CONTACT
H
HAESEBAERT Julie, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
1
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