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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT00828217
Other study ID # AC-2008-HO
Secondary ID
Status Recruiting
Phase N/A
First received January 22, 2009
Last updated September 23, 2010
Start date November 2008
Est. completion date November 2010

Study information

Verified date September 2010
Source Central Hospital, Nancy, France
Contact Elodie Speyer, PhD student
Phone +33383683558
Email elodie.speyer@medecine.uhp-nancy.fr
Is FDA regulated No
Health authority France: Institutional Ethical CommitteeFrance: Afssaps - Agence française de sécurité sanitaire des produits de santé (Saint-Denis)
Study type Interventional

Clinical Trial Summary

The aim of this study is to assess the efficacy of adapted physical activity intervention on health-related quality of life and satisfaction with care in hospitalized children and adolescents.

This is a randomized controlled study. The hypothesis is that children practicing adapted physical activity during their hospitalization present a higher health-related quality of life and satisfaction with care than those who do not.


Recruitment information / eligibility

Status Recruiting
Enrollment 312
Est. completion date November 2010
Est. primary completion date November 2010
Accepts healthy volunteers No
Gender Both
Age group 5 Years to 18 Years
Eligibility Inclusion Criteria:

- Length of hospital stay (more than 3 days)

- Children or parents able to understand and read French

- No medical contra-indications to physical activity

- Children hospitalized in 3 specific departments at Nancy Children's Hospital:

- Médecine Infantile 1 et 3(paediatrics)

- Médecine Infantile 2 (haematology-oncology, immunology department)

- Chirurgie orthopédique et Brûlés (orthopaedic surgery and Burned)

- Children and parents being agree to participate in the study

Exclusion Criteria:

- No written informed consent

- Children hospitalized less than 3 days

- Medical contra-indication to physical activity

- Children already included in that study (former hospitalization)

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label


Related Conditions & MeSH terms


Intervention

Other:
adapted physical activity
one session of adapted physical activity per day (30 minutes each session), during the whole stay at the hospital

Locations

Country Name City State
France University Hospital, Children's Hospital Vandoeuvre Les Nancy

Sponsors (3)

Lead Sponsor Collaborator
Central Hospital, Nancy, France Association pour la promotion du sport chez l'enfant malade (APSEM), University of Nancy

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary health-related quality of life measurement 2 points: on the first and last day of hospitalization No
Secondary satisfaction with care measurement 1 point: 15 days after hospital discharge No
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