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Influence of a Residential Rehabilitation Program on Body Composition in Patients with Cystic Fibrosis

Influence of a Residential Rehabilitation Program on Body Composition in Patients with Cystic Fibrosis (children and Adults)

Status
Terminated
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04527796
Enrollment
39
Registered
2020-08-27
Start date
2018-09-01
Completion date
2020-07-01
Last updated
2024-09-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cystic Fibrosis

Keywords

body composition, rehabilitation

Brief summary

The aim is to evaluate the impact of a 3-week lasting residential rehabilitation program for patients with cystic fibrosis on their nutritional status measured as BMI and body composition and pulmonary function.

Detailed description

Cystic fibrosis Patients following a residential rehabilitation program consisting of dietary adaptation, physical therapy for airway drainage and supervised inhalation therapy and physical activity for at least 3 weeks are asked to participate. Weight, height, body composition and pulmonary function will be measured at start and end of the program. Dietary intake during the program is calculated based on a 2 day weighed intake diary and physical activity will be measured with the SenseWear pro 3 armband.

Interventions

OTHERRehabilitation

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.

Sponsors

University Hospital, Ghent
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
6 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Cystic fibrosis * stay at the rehabilitation center for at least 3 consecutive weeks

Exclusion criteria

* steroid use * absence from the program for more than 2 consecutive days

Design outcomes

Primary

MeasureTime frameDescription
body composition changeday 0 and day 21 (start and end of the rehabilitation program)Dual energy X-ray absorptiometry measured Fat mass index (kg/m\*2)
Body mass index changeday 0 and day 21 (start and end of the rehabilitation program)calculated based on weight and height (kg/m\*2) converted in standard deviations
Weight changeday 0 and day 21 (start and end of the rehabilitation program)Scale weighed weight (kg) converted in standard deviations of normal population of normal populations
pulmonary function changeday 0 and day 21 (start and end of the rehabilitation program)forced expiratory volume in 1 second (% of normal)

Secondary

MeasureTime frameDescription
Physical activityWeek 1SenseWear pro 3 armband measured physical activity
dietary intake2 days/week for 3 consecutive weeksmacronutrient intake measured based on 2 days/week weighed nutritional intake

Countries

Belgium

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 24, 2026