Actively Recruiting

Phase Not Applicable
Age: 6Years - 18Years
All Genders
NCT07001631

Effect of EMDR for Reduction of Pain Interference in Children With Sickle Cell Disease

Led by Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA) · Updated on 2025-06-03

40

Participants Needed

1

Research Sites

144 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Children with sickle cell disease may experience frequent painful episodes. This, together with the traumatic experiences during a hospitalization, can lead to the development of posttraumatic stress reactions. As the stress can trigger painful episodes (pain crisis) in children with sickle cell disease, the investigators think that treating these stress symptoms can reduce the pain-related problems in their lives. Eye Movement Desensitization and Reprocessing (EMDR) is proven to be an effective trauma treatment for posttraumatic stress disorder. Research studies show that EMDR can reduce pain in adults. The investigators want to study now if EMDR effective is in reducing pain-related problems in children with sickle cell disease.

CONDITIONS

Official Title

Effect of EMDR for Reduction of Pain Interference in Children With Sickle Cell Disease

Who Can Participate

Age: 6Years - 18Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Medical diagnosis of sickle cell disease
  • Age between 6 and 18 years old
  • Elevated pain interference scores above the clinical cut-off T-score of 49 on PROMIS Pain Interference (parent-proxy version for children 6-7 years and self-report for children 8 years and older)
  • Sufficient knowledge of Dutch or English to complete assessments
Not Eligible

You will not qualify if you...

  • Undergone successful stem cell transplantation
  • Pregnant adolescents
  • Current unsafety likely to interfere with therapy, such as ongoing domestic violence
  • Major acute medical or psychiatric condition interfering with participation, including psychosis, substance dependence, severe self-harm, or high suicide risk requiring immediate treatment
  • Receiving psychological trauma treatment by another therapist
  • Estimated IQ below 80 based on medical or educational records

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Amsterdam UMC

Amsterdam, Netherlands

Actively Recruiting

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Research Team

M

Mariana Nery, MD

CONTACT

L

Linde Scholten

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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