Evaluation of the Effect of a Physical Activity Recovery Stay

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age8-18
SponsorUnion de Gestion des Etablissements des Caisses d'Assurance Maladie - Nord Est

About this trial

A WHO study in 2020 revealed that 81% of adolescents (aged 11-17) do not respect the recommendation of one hour of moderate physical activity per day. In the context of disability, many factors impose limits on physical activity. While the pathology itself induces limitations and restrictions (prolonged sitting time, assisted movement, etc.), organizational constraints also apply to both children and parents, who have to divide their time between work, school and therapeutic care, which is sometimes numerous and varied over the course of a single week. These limitations generate stress and fatigue, and prolonged sedentary periods lead children with chronic illnesses, rare diseases or disabilities into a process of physical deconditioning. The accumulation of sedentary time is detrimental to cardiovascular and metabolic health.

To combat this deconditioning, the 2008 National Physical Activity and Sport Plan (PNAPS) sets out the main guidelines for treatment and implementation. The plan explains that "for patients with chronic illnesses, rare diseases or disabilities, the aim is to encourage care and guidance towards Adapted Physical Activity (APA). The attending physician will be able to identify local therapeutic education programs, rehabilitation services and "sport-santé" offers, to improve access for these patients to supervised local programs". In addition, the plan suggests "developing APA programs in healthcare establishments to enable people with chronic illnesses, rare diseases or disabilities to access health education incorporating practical sessions".

In line with this plan, an exercise reconditioning program has been set up at our facility. This three-month stay includes children with a variety of pathologies, but with a common feature of physical deconditioning.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Children with a pathology (chronic disease, rare disease or disability) in a state of deconditioning to exercise

Taken in charge at the CMPRE for a stay to resume physical activity

Disqualifiers

Age under 8 and over 18

Patients undergoing rehabilitation during the stay

Patients with a significant change in their therapeutic management during the stay

Significant cognitive impairment preventing comprehension of instructions

Trial population

The children taking part in the return-to-physical-activity program are referred to the Flavigny-sur-Moselle CMPRE for medical consultation due to a state of deconditioning to physical exertion concomitant with a pathological situation. The pathology most frequently encountered during this stay is cerebral palsy. However, the Flavigny CMPRE is accredited in a number of fields (orthopedics, burns, neurology, oncology), and the pathologies of the children referred to this stay are representative of these. These include children with scoliosis, obesity, Guillain-Barré syndrome, cystic fibrosis, Charcot's disease and cancer.

Trial design

Design model

Other

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

50 Participants
are grouped into 1 trial group
Group A: Deconditioning to physical exertion

Trial outcomes

Primary outcomes

1

Diagnoform test score

To evaluate the effect of the return to physical activity stay prescribed by the doctors at the Flavigny CMPRE on the physical condition of the children taking part in the stay Score between 0 and 20 for each part of the test, with 20 being the best score (and therefore the best physical condition).

Time frame
Day of patient inclusion and 3 months after, day on which the study ends for the patient

Secondary outcomes

1

KidScreen52 quality-of-life scale score.

Quality of life scale : a T-score value is calculated. Scores range from 10 to 50, where 10 represents the lowest possible value and thus a very low health-related quality of life and 50 the maximum value, i.e. a very high health-related quality of life.

Time frame
Day of patient inclusion and 3 months after, day on which the study ends for the patient
2

Impedance measurement

Recording weight on a balance : Ideally, the patient should have lost weight by the end of the reconditioning stay.

Time frame
Day of patient inclusion and 3 months after, day on which the study ends for the patient
3

Exercise test on ergometer

Three-minute warm-up without resistance, then increase in difficulty every minute until you reach 80% of your theoretical maximum heart rate.

Time frame
Day of patient inclusion and 3 months after, day on which the study ends for the patient
4

Anamnesis

description of the antecedents

Time frame
Day of patient inclusion and 3 months after, day on which the study ends for the patient

Other outcomes

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