Influence of a Residential Rehabilitation Program on Body Composition in Patients with Cystic Fibrosis
NCT ID: NCT04527796
Last Updated: 2024-09-19
Study Results
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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TERMINATED
39 participants
OBSERVATIONAL
2018-09-01
2020-07-01
Brief Summary
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Detailed Description
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Conditions
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Study Design
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OTHER
RETROSPECTIVE
Study Groups
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rehabilitation
All included patients get an pre-intervention and a post intervention analysis
Rehabilitation
During the rehabilitation program a multidisciplinary team, consisting of a pneumologist, dietician, psychologist, social worker and several physiotherapists, coach the cystic fibrosis patients.
The physiotherapists help with autogenic drainage and aerosol therapy (2-3 times/day) and supervise physical activity (5, 1-hour lasting, training sessions/week: swimming 2, Fitness training 2, 1 session of choice). The dietician calculates basal and theoretical energy needs . A carbohydrate-rich snack before exercise, to improve exercise tolerance and a carbohydrate-protein-rich snack afterwards to improve recuperation is provided.
Interventions
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Rehabilitation
During the rehabilitation program a multidisciplinary team, consisting of a pneumologist, dietician, psychologist, social worker and several physiotherapists, coach the cystic fibrosis patients.
The physiotherapists help with autogenic drainage and aerosol therapy (2-3 times/day) and supervise physical activity (5, 1-hour lasting, training sessions/week: swimming 2, Fitness training 2, 1 session of choice). The dietician calculates basal and theoretical energy needs . A carbohydrate-rich snack before exercise, to improve exercise tolerance and a carbohydrate-protein-rich snack afterwards to improve recuperation is provided.
Eligibility Criteria
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Inclusion Criteria
* stay at the rehabilitation center for at least 3 consecutive weeks
Exclusion Criteria
* absence from the program for more than 2 consecutive days
6 Years
ALL
No
Sponsors
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University Hospital, Ghent
OTHER
Responsible Party
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Principal Investigators
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Stephanie Van Biervliet, MD, PhD
Role: PRINCIPAL_INVESTIGATOR
Gent university hospital
Locations
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Zeepreventorium de Haan
De Haan, , Belgium
Countries
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Other Identifiers
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B670201939582
Identifier Type: -
Identifier Source: org_study_id
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