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

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age8+
SponsorUniversity of Liege

About this trial

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

This trial accepts healthy volunteers

Qualifiers

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

To have a child who suffer from cancer

Disqualifiers

/

Trial design

Design model

Parallel

Treatments tested in this trial

  • Self care + Hypnosis group

    Behavioral

    Our groupal intervention is divided into 6 monthly 2-hour sessions in which some self-hypnosis exercises are proposed to participants. Self-care techniques are also discussed (knowing our own needs, self-respect, assertiveness, coping with ruminations...) and homework assignments are proposed to participants, in order to foster positive change.

Treatment groups

30 Participants
are divided into 2 treatment groups
Group A: Children with cancer + their siblingsExperimental treatment 1 intervention
Group B: Parents of children with cancerExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Change in children's quality of life

Self-assessment of children's quality of life. Measured with the Pediatric Quality of Life Inventory-Cancer Module (PedsQL-3.0-Cancer) and the Pediatric Quality of Life Inventory-Core Module (PedsQL-4.0-Core). Children with cancer answer to both questionnaires but their siblings only answer the PedsQL-4.0-Core.

Time frame
T0 (before the intervention), T1 (right after the intervention : 6 months later)
2

Change in parents' conception of their child's quality of life

Parents' hetero-evaluation of the child's quality of life. Measured with the Parental version of the Pediatric Quality of Life Inventory-Cancer Module (PedsQL-3.0-Cancer) and the Parental version of the Pediatric Quality of Life Inventory-Core Module (PedsQL-4.0-Core).

Time frame
T0 (before the intervention), T1 (right after the intervention : 6 months later)
3

Change in children's cancer-related fatigue

A sense of tiredness or exhaustion linked with cancer and its treatments, that is not alleviated by sleep. Measured with the Pediatric Functional Assessment of Chronic Illness Therapy-Fatigue (pedsFACIT-F) among children with cancer and their siblings .

Time frame
T0 (before the intervention), T1 (right after the intervention : 6 months later)
4

Change in parents' fatigue

Measured with the Multidimensional Fatigue Inventory (MFI-20).

Time frame
T0 (before the intervention), T1 (right after the intervention : 6 months later)

Secondary outcomes

1

Change in the family impact of the cancer

Impact of the child's health on the parents' quality of life and on the familily fonctioning. Measured with the Pediatric Quality of Life Inventory-Family Impact Module (PedsQL-2.0-Family Impact Module)

Time frame
T0 (before the intervention), T1 (right after the intervention : 6 months later)
2

Change in parents' emotional distress

Anxiety and depression of the parents measured with the Hospital Anxiety and Depression Scale (HADS)

Time frame
T0 (before the intervention), T1 (right after the intervention : 6 months later)
3

Change in parents' coping strategies

The way parents cope adverses events. Measured with Ways of Coping Checklist (WWC-R)

Time frame
T0 (before the intervention), T1 (right after the intervention : 6 months later)

Other outcomes

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