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Adapted Physical Activity Program (APA) for Effort Rehabilitation of Children and Teenagers With Osteogenesis Imperfecta (BONeMOVE)

Primary Purpose

Osteogenesis Imperfecta

Status
Not yet recruiting
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Adapted Physical Activity program
Sponsored by
University Hospital, Toulouse
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Osteogenesis Imperfecta focused on measuring Osteogenesis Imperfecta, Children, Adolescents, Maximum oxygen consumption, Adapted physical activity, Effort rehabilitation

Eligibility Criteria

7 Years - 18 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Diagnosed Osteogenesis Imperfecta Informed and written consent signed by at least one of the two holders of parental authority Patient affiliated to a social security scheme or equivalent Exclusion Criteria: Non-walking children (unable to perform the effort test) Pregnant or breastfeeding Participation in other interventional research

Sites / Locations

  • CHU Toulouse

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Experimental group: 6 months APA program

Arm Description

The various assessments will be carried out during 2 visits at 6 months interval as part of the usual follow-up at the "Constitutional Bone Diseases" unit at the Toulouse University Hospital. The APA program built from the initial assessment will be returned to the child and his family during a videoconference. In addition, a regular reassessment and adjustment of this program will be made every 15 days during phone calls by the APA coach.

Outcomes

Primary Outcome Measures

Change from Baseline maximum endurance capacity at 6 months
Maximum oxygen consumption (VO2 peak) during an exercise test will be measured

Secondary Outcome Measures

Change from baseline quality of life questionnaire score at 6 months
Osteogenesis Imperfecta Specific Quality of Life Questionnaire (OIQoL). Total scores are based on a 0-100 scale, where a high score represents better quality of life
Change from baseline number of steps at 6 months
6-minute walk test (6MWT) assessed by connected watch
Change from baseline Weight at 6 months
Body Mass Index

Full Information

First Posted
June 13, 2023
Last Updated
June 27, 2023
Sponsor
University Hospital, Toulouse
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1. Study Identification

Unique Protocol Identification Number
NCT05927389
Brief Title
Adapted Physical Activity Program (APA) for Effort Rehabilitation of Children and Teenagers With Osteogenesis Imperfecta
Acronym
BONeMOVE
Official Title
BONeMOVE : an Adapted Physical Activity Program (APA) for Effort Rehabilitation of Children and Teenagers With Osteogenesis Imperfecta: an Interventional, Prospective, Regional, Bicentric Study.
Study Type
Interventional

2. Study Status

Record Verification Date
June 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
July 15, 2023 (Anticipated)
Primary Completion Date
July 15, 2025 (Anticipated)
Study Completion Date
July 15, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Toulouse

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This research study aims to evaluate the effect of a 6-month adapted physical activity program (APA) on the endurance capacities (evaluated as the maximum oxygen consumption [VO2 peak]) of children and adolescents with Osteogenesis Imperfecta.
Detailed Description
Osteogenesis Imperfecta (OI) is a rare genetic disease characterised mainly by bone fragility, decreased bone mass and a susceptibility to fractures of varying severity. Different forms have been described according to the severity of the bone manifestations. Although it is a genetically heterogeneous disease, approximately 90% of OI patients have a mutation in the gene encoding gene encoding type 1 collagen, a major component of the extracellular matrix. Chronic fatigue and decreased physical endurance are almost constant complaints of patients with OI (more than 95% according to some studies), which impacts the activities of daily living and quality of life of these patients. The causes of this decrease in endurance are multifactorial involving prolonged immobilisation secondary to fractures, chronic osteoarticular pain, but also primary muscle damage. Mechanography studies carried out in children with OI have shown a significant deficit in muscle function in terms of both strength and power. In healthy adults, physical inactivity is an important predictor of feeling of tired. In addition, in some chronic diseases (such as multiple sclerosis, rheumatoid arthritis or systemic lupus erythematosus), physical activity and training have been shown to be effective in improving muscle strength and functional capacity as well as fatigue and quality of life. In OI, it has been reported that physical activity improves muscle function and bone mass. Patients with OI should therefore benefit from a regular exercise programme taking into account their risk of fracture. This study aims to evaluate the effect of a life-skills physical activity (LSPA) programme on the endurance capacities and quality of life of children and adolescents with OI. The VO2 peak evolution will be evaluated after 6 months of program. This is a recognized parameter for the evaluation of endurance and has been validated in children. The hypothesis of this study is that the implementation of a physical activity program adapted to the daily life and interests of the child with OI will efficiently improve endurance, prevent deconditioning and promote long term benefits.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Osteogenesis Imperfecta
Keywords
Osteogenesis Imperfecta, Children, Adolescents, Maximum oxygen consumption, Adapted physical activity, Effort rehabilitation

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
30 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Experimental group: 6 months APA program
Arm Type
Experimental
Arm Description
The various assessments will be carried out during 2 visits at 6 months interval as part of the usual follow-up at the "Constitutional Bone Diseases" unit at the Toulouse University Hospital. The APA program built from the initial assessment will be returned to the child and his family during a videoconference. In addition, a regular reassessment and adjustment of this program will be made every 15 days during phone calls by the APA coach.
Intervention Type
Other
Intervention Name(s)
Adapted Physical Activity program
Intervention Description
The Adaptated Physical Activity program consists of a Personalized Training Program adapted to each patient's condition and capacities
Primary Outcome Measure Information:
Title
Change from Baseline maximum endurance capacity at 6 months
Description
Maximum oxygen consumption (VO2 peak) during an exercise test will be measured
Time Frame
Change from Baseline to 6 months
Secondary Outcome Measure Information:
Title
Change from baseline quality of life questionnaire score at 6 months
Description
Osteogenesis Imperfecta Specific Quality of Life Questionnaire (OIQoL). Total scores are based on a 0-100 scale, where a high score represents better quality of life
Time Frame
Change from Baseline to 6 months
Title
Change from baseline number of steps at 6 months
Description
6-minute walk test (6MWT) assessed by connected watch
Time Frame
Change from Baseline to 6 months
Title
Change from baseline Weight at 6 months
Description
Body Mass Index
Time Frame
Change from Baseline to 6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
7 Years
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Diagnosed Osteogenesis Imperfecta Informed and written consent signed by at least one of the two holders of parental authority Patient affiliated to a social security scheme or equivalent Exclusion Criteria: Non-walking children (unable to perform the effort test) Pregnant or breastfeeding Participation in other interventional research
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Thomas EDOUARD, MD
Phone
05 61 77 61 10
Email
edouard.t@chu-toulouse.fr
First Name & Middle Initial & Last Name or Official Title & Degree
Marjolaine WILLEMS, MD
Email
m-willems@chu-montpellier.fr
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Thomas EDOUARD, MD
Organizational Affiliation
CHU Toulouse
Official's Role
Principal Investigator
Facility Information:
Facility Name
CHU Toulouse
City
Toulouse
Country
France
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Thomas EDOUARD, MD
Phone
05 61 77 61 10
Email
edouard.t@chu-toulouse.fr

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
458828
Citation
Sillence DO, Senn A, Danks DM. Genetic heterogeneity in osteogenesis imperfecta. J Med Genet. 1979 Apr;16(2):101-16. doi: 10.1136/jmg.16.2.101.
Results Reference
background
PubMed Identifier
31693577
Citation
Rossi V, Lee B, Marom R. Osteogenesis imperfecta: advancements in genetics and treatment. Curr Opin Pediatr. 2019 Dec;31(6):708-715. doi: 10.1097/MOP.0000000000000813.
Results Reference
background
PubMed Identifier
20856683
Citation
Monti E, Mottes M, Fraschini P, Brunelli P, Forlino A, Venturi G, Doro F, Perlini S, Cavarzere P, Antoniazzi F. Current and emerging treatments for the management of osteogenesis imperfecta. Ther Clin Risk Manag. 2010 Sep 7;6:367-81. doi: 10.2147/tcrm.s5932.
Results Reference
background
PubMed Identifier
29310646
Citation
Arponen H, Waltimo-Siren J, Valta H, Makitie O. Fatigue and disturbances of sleep in patients with osteogenesis imperfecta - a cross-sectional questionnaire study. BMC Musculoskelet Disord. 2018 Jan 8;19(1):3. doi: 10.1186/s12891-017-1922-5.
Results Reference
background
PubMed Identifier
31900144
Citation
Harsevoort AGJ, Gooijer K, van Dijk FS, van der Grijn DAFM, Franken AAM, Dommisse AMV, Janus GJM. Fatigue in adults with Osteogenesis Imperfecta. BMC Musculoskelet Disord. 2020 Jan 3;21(1):6. doi: 10.1186/s12891-019-3000-7.
Results Reference
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Adapted Physical Activity Program (APA) for Effort Rehabilitation of Children and Teenagers With Osteogenesis Imperfecta

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