Implementation and Effectiveness of a Community-based Exercise on Prescription Program for Adults With Chronic Diseases

NCT ID: NCT04919889

Last Updated: 2025-03-26

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

330 participants

Study Classification

OBSERVATIONAL

Study Start Date

2017-09-01

Study Completion Date

2020-09-10

Brief Summary

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The objectives were (1) to evaluate the characteristics of the patients referred, and (2) the effect of a community-based Exercise on Prescription program on their physical capacities and their quality of life.

The program consisted in 30 supervised physical activity (PA) group sessions (75 min) over a 4-month period and participant were prescribed the program by their doctors.

The participants had chronic diseases among type 2 diabetes, mental disorders, musculoskeletal disorders, childhood and adult obesity and stabilized cardiovascular diseases.

Tests and questionnaires were completed before and after the program. Physical tests were the 6-minute walk test, the timed up \& go, the 30-s stand up chair, the single leg support test and the back scratch and toe-touch tests. Questionnaires were the self-administered Ricci and Gagnon questionnaire about PA level and the 12-Item Short Form Survey for measuring quality of life.

Personal goal from the participants and medical objective from their doctors were collected before the program.

Detailed Description

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Conditions

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Prescription Physical Activity Chronic Disease

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Interventions

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Exercise prescription

All individuals referred to the community-based Exercise on Prescription program

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* All participant referred to the Exercise on Prescription Program (Caen)

Exclusion Criteria

* French language not sufficiently read and/or spoken
* Lack of clear information on the study
* Alteration of higher functions or sensory disturbance making understanding and adherence to the research protocol impossible.
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University Hospital, Caen

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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CHU Caen Normandie

Caen, , France

Site Status

Countries

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France

Other Identifiers

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SSOCaen

Identifier Type: -

Identifier Source: org_study_id

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