Adhesion of Children and Adolescents Treated for Cancer to Personalized Support in Adapted Physical Activity Program (APADHOP)

January 30, 2024 updated by: University Hospital, Grenoble

Evaluation of the Adhesion of Children and Adolescents Treated for Cancer to Personalized Support in Adapted Physical Activity

Adapted physical activity session with a formed professional is proposed in standard care since 2022 in the immuno-hematological service to all children with newly diagnosed cancer or relapse.

The aim of this study is to keep the children in the APA programm during all the treatment lenght.

This study aims to evaluate by questionnaires the motivation keys and restraint from children and parents before the APA program starts (at diagnosis or relapse if not previously participating to an APA programm) and after 4 to 6 months of APA programm.

The final expected fallout is to enhance children adhesion to long term APA program by implementing tools in current practice to overcome restraints from young patients and their parents

Study Overview

Detailed Description

The literature and the French Cancer Plan confirm the benefits of physical activity for cancer patients, and underline the importance of developing appropriate physical activity support for children and adolescents, given their specific needs and the societal and public health challenge represented by these budding patients.

Despite the abundance of studies relating to physical activity in oncology, few data are available, particularly in the pediatric and adolescent/young adult population :

  • on physical activity interventions initiated early and sustained over time
  • on personalized physical activity interventions integrated into the patient's care/life trajectory
  • on factors favoring adhesion to an adapted physical activity program [APA] during and/or after cancer treatment

This is a prospective, exploratory, monocentric study to explore these points.

As part of routine management in the immunohaemato-oncology [IHO] department of the Grenoble Alpes University Hospital, a personalized physical activity [PA] program is systematically proposed by a PA professional, with a program adapted to the child, his or her motivations and limitations.

As part of the protocol, a questionnaire-based assessment of motivations and obstacles, as well as quality of life, will be carried out at the start of the PA program and again after 4 to 6 months. Criteria for adherence to the APA program will also be collected.

EXPECTED OUTPUTS

  • Propose an organizational model in pediatric oncology for the early and sustained practice of APA with children and adolescents hospitalized for cancer.
  • Finalize assessment and follow-up materials for children receiving APA support in pediatric oncology (information leaflets, certificate of no contra-indication to APA, assessment and follow-up form, questionnaire on attitude and motivation to APA, etc.).
  • Provide guidance to help young cancer patients adhere more effectively to APA program.
  • Participate in the promotion of APA and the development of APA recommendations for children and adolescents treated for cancer, in conjunction with the SFCE (Children Cancer French Society) national working group on APA for children and adolescents with cancer.

Study Type

Observational

Enrollment (Estimated)

48

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

    • Isere
      • Grenoble, Isere, France, 38000
        • CHU Grenoble Alpes
        • Sub-Investigator:
          • cécile perret
        • Contact:
        • Contact:
        • Sub-Investigator:
          • Mélanie balleeger
        • Sub-Investigator:
          • anne pagnier
        • Sub-Investigator:
          • gaelle stofleth
        • Sub-Investigator:
          • corinne armari alla
        • Sub-Investigator:
          • severine bobillier chaumont
        • Sub-Investigator:
          • dalila adjaoud
        • Principal Investigator:
          • Leila Gofti Laroche

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

Children with cancer taken in charge in the paediatric immuno haematology service of the Grenoble Alpes University Hospital

Description

Inclusion Criteria:

  • Patients aged 3 years to under 18 years under care at Grenoble Alpes University Hospital
  • New cancer diagnosis or relapse in the absence of previous APA treatment
  • All cancer pathologies:

Diagnosis of acute or chronic hematological malignancy OR Central nervous system tumors OR Other solid tumors

  • Regardless of therapeutic pathway
  • Patient and parents who have not objected to participation after being informed

Exclusion Criteria:

  • Patient with a strict medical contraindication to physical activity identified by the referring physician or another specialist physician, particularly the sports physician (unstabilized heart or lung disease, uncontrolled diabetes, etc.)

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Adhesion to an APA programm
Time Frame: 4 to 6 months
Adherence of children and adolescents undergoing cancer treatment to personalized support in Adapted Physical Activity [APA] offered at an early stage and for a minimum duration of 4 to 6 months : patients following the whole APA program/patients included, in percent
4 to 6 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Motivation and restraints
Time Frame: 4 to 6 months

This outcome is measured through a semi directive questionnaire elaborated by the SENS laboratory (Laboratory of physical exercice and social environment, Grenoble, France). It measures attitudes and motivations that have been identified as key factors in behavior change, within the framework of the main health psychology models of behavior change, such as the theory of planned behavior, the health action process approach, or self-determination theory .In order to measure these constructs, tools adapted to children from 8 years old and scientifically validated were identified in the scientific literature and adapted for the APADHOP project.

Children with cancer over 8 years old and one or both parents will answer to questions at the start of the adapted physical activity programm ((APA) and after 4 to 6 months of APA personnalised support.

There is no scoring as this is a descriptive outcome (after been analyzed by a humanities and social sciences researcher)

4 to 6 months
Quality of life measure
Time Frame: 4 to 6 months

Quality of life will be measured by international validated PedsQL questionnaires V4.0 (paediatric quality of Life Inventory) according to the age of the patient:

  • For parents of children aged 2-4 years:
  • For parents of children aged 5 to 7
  • For parents of children aged 8 to 12
  • For parents of children aged 13 to 18
  • For children aged 5 to 7
  • For children aged 8 to 12
  • For children aged 13 to 18 This questionnaires will be administrated at the start of the adapted physical activity (APA) programm and after 4 to 6 months of personalized APA support.

Each item of the questionnaire is scored between 0 and 4 and the total score of the questionnaire is between 0 an 100. The higher score means a better quality of life.

To be able to measure the score at least 50% of the items must be answered. The results will be analysed only for patients and parents who have answered to the questionnaires at both evaluation time.

4 to 6 months
Representation of physical activity
Time Frame: 4 to 6 months

The evaluation of the representation of physical activity Activity of children and parents at diagnosis and after 4 to 6 months of personalized APA support will be performed through a semi directive questionnaire elaborated by the SENS Laboratory (Laboratory of physical exercice and social environment, Grenoble University in France).

The questionnaires will be administred to patients over 8 years and parents at the start of the adapted physical activity (APA) programm and after 4 to 6 months of personalized APA support. The effect of personalized support will also be studied by carrying out pre/post analyzes of these dimensions.

There is no scoring as this is a descriptive outcome that will be analysed by humanities and social siences university researchers.

4 to 6 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Collaborators

Investigators

  • Principal Investigator: Leila Gofti Laroche, MD, CHU Grenoble Alpes

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Estimated)

February 1, 2024

Primary Completion (Estimated)

August 1, 2024

Study Completion (Estimated)

January 31, 2025

Study Registration Dates

First Submitted

December 26, 2023

First Submitted That Met QC Criteria

January 26, 2024

First Posted (Actual)

January 29, 2024

Study Record Updates

Last Update Posted (Estimated)

February 1, 2024

Last Update Submitted That Met QC Criteria

January 30, 2024

Last Verified

December 1, 2023

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 2023-A02343-42

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

No individual participant data sharing

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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