Adaptation Strategies for Coping With the Impact of Sensory Alterations on Eating Behavior in Children With Cancer: A Qualitative Study From the Perspective of Children and Parents

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age6-17
SponsorCentre Leon Berard

About this trial

Childhood cancer is a serious and life-changing disease that affects thousands of children every year worldwide. In addition to the disease itself, cancer treatments such as chemotherapy often cause difficult side effects. Among these, changes in taste and smell are very common but still poorly understood in children. These sensory changes can make food taste unpleasant or smell different, leading children to eat less, avoid certain foods, or develop strong food aversions. As a result, many children with cancer experience weight loss, poor nutrition, and reduced quality of life, which can also affect how well they tolerate treatment.

Research suggests that between 40% and 60% of children with cancer struggle to maintain good nutritional status during treatment. Taste and smell alterations play a major role in these difficulties. Children may experience nausea triggered by food smells, changes in food texture perception, or a loss of pleasure in eating. Parents often report feeling powerless and lacking clear guidance on how to help their child cope with these problems.

While taste and smell disturbances have been widely studied in adults with cancer, much less is known about how children experience these changes and, importantly, how they and their families adapt to them. Parents play a key role in supporting their child's eating habits, but their perspectives may differ from the child's own experiences.

This study aims to better understand how children undergoing chemotherapy and their parents perceive changes in taste, smell, and food texture, and how these changes affect eating behavior, emotions, and social life. Using individual semi-structured interviews, the study will explore the coping strategies used by children and parents to manage these sensory changes, both at home and in the hospital setting.

By giving children and parents a voice, this research seeks to identify practical, real-life strategies that families find helpful. The results will contribute to improving nutritional support and guidance for children with cancer, with the ultimate goal of enhancing their well-being, quality of life, and treatment outcomes.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Aged 6 to 17 years old on the day consent is obtained.

Diagnosed with a malignant hematological or oncological tumor.

Possessing sufficient verbal ability to participate in the interview planned for the study.

Having started chemotherapy treatment at least 2 months prior.

Disqualifiers

None

Trial population

History of cancer Any cognitive impairment or condition that may limit the use of numerical scales and quality of life questionnaires, including but not limited to: Children with neurodevelopmental disorders such as autism or Down syndrome These children may have specific cognitive or communication characteristics that require specialized interview techniques. Their inclusion could complicate data comparability and introduce confounding factors. This exclusion ensures data quality and consistency, while respecting the well-being of participants. Patients for whom other types of cancer treatment are planned during the study period (e.g., radiation therapy) Patients in relapse Presence of a pre-existing pediatric eating disorder or pre-existing food selectivity

Trial design

Design model

Case-only

Time perspective

Other

Treatments tested in this trial

  • No Intervention: Observational Cohort

    Behavioral

    no intervention

Treatment groups

30 Participants
are divided into 2 treatment groups
Group A: children aged 6-17 years undergoing chemotherapy for a malignant hematological or solid tumor1 intervention
Group B: one of the parent of the children included in the first group1 intervention

Trial outcomes

Primary outcomes

1

coping strategies of the children and their parents for managment of sensory alterations and eating behaviour

Determine the coping strategies used by children and their parents to manage sensory alterations and eating behavior during chemotherapy. the method for the thematic analysis of qualitative data described by Braun and Clarke will be used

Time frame
at least 2 months after the beginning of the chemotherapy

Secondary outcomes

1

Determine the effectiveness and purpose of these strategies.

the method for the thematic analysis of qualitative data described by Braun and Clarke will be used

Time frame
at least 2 months after the beginning of the chemotherapy
2

Characterize the sensory alterations reported by children undergoing chemotherapy

the method for the thematic analysis of qualitative data described by Braun and Clarke will be used

Time frame
at least 2 months after the beginning of the chemotherapy
3

Identify the frequency, reported intensity, and duration of alterations in taste, smell, and texture, and their role in eating behavior in children undergoing chemotherapy.

the method for the thematic analysis of qualitative data described by Braun and Clarke will be used

Time frame
at least 2 months after the beginning of the chemotherapy
4

Determine the influence of cancer type and eating environment (hospital or home) on food perception

the method for the thematic analysis of qualitative data described by Braun and Clarke will be used

Time frame
at least 2 months after the beginning of the chemotherapy

Other outcomes

Sponsors and contacts

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Centre Leon Berard

Lead sponsor

Nutricia, Inc.

Collaborator

This trial is not recruiting at the moment. You can still explore other options: