← Back to Clinical Trials
Recruiting NCT03435042

NCT03435042 A Hypnosis-based Group Intervention to Improve Quality of Life in Children With Cancer and Their Parents.

◆ AI Clinical Summary
Plain-language summary for patients
Clinical Trial Summary
NCT ID NCT03435042
Status Recruiting
Phase
Sponsor University of Liege
Condition Pediatric Cancer
Study Type INTERVENTIONAL
Enrollment 30 participants
Start Date 2018-01-25
Primary Completion 2028-12-31

Eligibility & Interventions

Sex All sexes
Min Age 8 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
Self care + Hypnosis group

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 30 participants in total. It began in 2018-01-25 with a primary completion date of 2028-12-31.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

Background: A lot of children with cancer suffer from emotional distress, fatigue and relational difficulties. Their parents are also impacted by the disease: their responsibilities increase and they can feel more distressed and tired. Different psychological interventions designed for ill children and their parents seem to be efficient to improve their social functioning, coping strategies and well-being. However, more research is needed in this field. Hypnosis is often used in paediatric oncology, mostly to decrease procedure-related pain and distress. It has been used efficiently to improve the well-being of adults with cancer. This paper describes a pilot study designed to assess the feasibility and interest of a group intervention combining self-care and hypnosis for children with cancer and their parents, and a quasi-experimental protocol aimed at assessing the efficacy of this group intervention to improve the quality of life of children and their parents. Methods: Our pilot study showed that our intervention was feasible and positive for the participants. To test the efficacy of the intervention, two groups will be set up: one with children with cancer and their interested siblings, and one with their parents. Data will be collected for each group before and after the intervention by questionnaires and a semi-structured interview. Discussion: There is a growing interest in hypnosis in oncology settings. The results of this study should improve knowledge about the efficacy of a group intervention combining self-care and hypnosis to improve quality of life of children with cancer and their family.

Eligibility Criteria

Inclusion Criteria: * Children and their siblings: * To be 8 to 18 year-old * To suffer from cancer (all localisations, stage and treatments accepted) or to have a sibling who suffer from cancer * To speak french * Parents: * To have a child who suffer from cancer * To speak french Exclusion Criteria: * /

Contact & Investigator

Central Contact

Charlotte Grégoire

✉ ch.gregoire@uliege.be

📞 043662398

Principal Investigator

Marie-Elisabeth Faymonville

STUDY DIRECTOR

Centre Hospitalier Universitaire de Liege

Frequently Asked Questions

Who can join the NCT03435042 clinical trial?

This trial is open to participants of all sexes, aged 8 Years or older, studying Pediatric Cancer. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT03435042 currently recruiting?

Yes, NCT03435042 is actively recruiting participants. Contact the research team at ch.gregoire@uliege.be for enrollment information.

Where is the NCT03435042 trial being conducted?

This trial is being conducted at Liège, Belgium.

Who is sponsoring the NCT03435042 clinical trial?

NCT03435042 is sponsored by University of Liege. The principal investigator is Marie-Elisabeth Faymonville at Centre Hospitalier Universitaire de Liege. The trial plans to enroll 30 participants.

Related Trials

Related Intelligence Guides

In-depth guides covering this condition's trials, eligibility, and what to expect.

ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology