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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT01433198
Other study ID # ML7560
Secondary ID
Status Withdrawn
Phase N/A
First received
Last updated
Start date May 2018
Est. completion date December 2020

Study information

Verified date November 2020
Source Universitaire Ziekenhuizen KU Leuven
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Aim: - to investigate the effects of an aquatic exercise program in patients with severe scars Patient population: - 10 patients of at least 18 years old - patients with scars after burns or other severe skin injuries - stratification into two groups: an intervention group and a control group Method: - 8 patients will participate in the aquatic exercise group and 2 patients in the control group - assessment of physical fitness parameters, scar tissue and psychosocial impact Hypothesis: - patients of the aquatic exercise group will recover sooner and better (physically and psychologically) than patients of the control group


Description:

Intervention: - during 6 weeks patients will performed an aquatic exercise program (2 to 3 sessions a week) Assessment: - T0: post-hospitalisation status: body mass index, physical fitness, strength and respiratory function - T1: at baseline: body mass index, physical fitness, strength, respiratory function, exercise capacity, mobility, scar parameters and some questionnaires - T2: after 6 weeks training: same measurements as T1 - T3: 3 months after end of aquatic training: idem T1 - T4: 6 months after end of aquatic training: questionnaires - T5: 1 year after end of aquatic training: questionnaires


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date December 2020
Est. primary completion date May 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - at least 18 years old - hospitalisation at the burn unit of at least 14 days - patients with severe skin damage (like burns, deglovements, necrotic fasciitis, ...) Exclusion Criteria: - younger than 18 years - psychiatric history (recommandation of psychiatrist not to participate in the study)

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Aquatic training
Aquatic training during a 6 weeks program (15 to 18 sessions of 1 hour)

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Universitaire Ziekenhuizen KU Leuven

Outcome

Type Measure Description Time frame Safety issue
Primary Change in physical activity using Dynaport activity monitor Post-hospitalisation status = participants will be followed during the last three consecutive days of their hospital stay.
The minimum period of hospital stay is 14 days (inclusion criteria), the maximum period of hospital stay is not determined. The expected average can not be given.
Post-hospitalisation status, baseline, after 6 weeks, after 3 months
Secondary Strength (Jamar, MicroFET, MIP) Strength (Jamar, MicroFET, MIP) Post-hospitalisation status, basline, after 6 weeks, after 3 months
Secondary Quality of life (using 5 questionnaires like SF-36) Quality of life (using 5 questionnaires like SF-36) Basline, after 6 weeks, after 3 months
Secondary Exercise capacity (6-minutes walking test and 4-minutes swimming test) Exercise capacity (6-minutes walking test and 4-minutes swimming test) Baseline, after 6 weeks and after 3 months
Secondary BMI BMI Post-hospitalisation status, baseline, after 6 weeks and after 3 months
Secondary Joint mobility Joint mobility Baseline, after 6 weeks, after 3 months
Secondary Pulmonary function (FEV1 and FVC) Pulmonary function (FEV1 and FVC) Post-hospitalisation status, baseline, after 6 weeks, after 3 months
Secondary Scar assessment Scar assessment Baseline, after 6 weeks, after 3 months
Secondary Physical fitness using Squash questionnaire Physical fitness using Squash questionnaire Baseline, after 6 weeks, after 3 months, after 6 months, after 1 year
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