Effects of an Individualized Exercise Program on Health-related and Skill/Performance-related fitness in CF.

January 2, 2019 updated by: Florian Stehling, University Hospital, Essen

Effects of an Individualized and Partially Supervised Exercise Program on Parameters of Physical Fitness, Lung Function, Habitual Physical Activity in Daily Life and Quality of Life in Children, Adolescents and Adults With Cystic Fibrosis.

The aim of this study is to evaluate the effects of a partially supervised exercise program on different aspects of physical fitness, despite VO2peak, lung function, quality of life and sleep quality in children, adolescents and adults with Cystic Fibrosis.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

There is growing consensus that exercise in subjects with cystic fibrosis (CF) may yield improvements in measures of physical fitness, lung function and quality of life. In most of the training studies exercise capacity was expressed as peak oxygen uptake (VO2peak), which has been found to be one of the best predictors of survival in subjects with CF. Those subjects with a higher VO2peak related to age and gender specific predicted VO2peak (%pred) have a better prognosis than those with a lower VO2peak (%pred). VO2peak represents the cardiorespiratory endurance is one aspect of physical fitness.

Physical fitness may be subdivided into health-related fitness and skill/performance-related fitness. Cardiorespiratory endurance, muscular strength and endurance, body composition and flexibility are often referred to as health-related fitness. Balance, coordination, speed, agility and power are often described as skill/performance related fitness, reflecting the performance aspect of physical fitness. It has been shown, that children and adolescents with a lower skill / performance related fitness are less physical active than those with a higher skill/performance related fitness. This may lead to physically inactive in daily life, less motivation to take part in organized sport and as a consequence to a lower VO2peak.

The primary outcome parameters of this study is to evaluate the effects 12-month partially supervised exercise program on 1) health-related fitness (endurance expressed as maximal workload, muscular strength) and skill / performance related fitness (balance, power, agility)and 2) habitual physical activity (steps / day; intensity expressed in METs) in a large group of subjects with CF. Secondary outcome parameters include forced exspiratory volume in 1 second (FEV1), sleep-wake cycle, quality of sleep, quality of life, and exercise related barriers and barrier management in physical exercise.

In total 100 subjects with CF 6 year and older will be included. Habitual physical activity and sleep will be recorded by accelerometer before subjects enter the exercise program, and after 6 month and after 12 month. Check-ups, lung function measurement and testing of physical fitness will be performed at baseline, after 6 and 12 month.

During the first six month the participants will be contacted by telephone every two weeks. After six month individual counseling by telephone will be stopped.

The exercise program is planned as a "low-threshold exercise program "with low barriers to participate. Participants will be asked about their interests and preferences of sports activities to conceive the exercise program together with the participants. Along with counseling participants will be motivated to increase physical activity by at least 10-20 minutes per day.

The investigators expect to gain another insight into different aspects of physical fitness, habitual physical activity and sleep from the results of this study. Up to know, there are only a few trails investigated different aspects of physical fitness that means balance, flexibility, power as parameters of health-related fitness and skill/performance-related fitness. The investigators assume that participants with higher values are more physical active than those with lower values and these participants will have a higher cardiorespiratory endurance.

Study Type

Interventional

Enrollment (Actual)

100

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Bochum, Germany, 44791
        • St. Josef-Hospital im Katholischen Klinikum Bochum, Klinik für Kinder und Jugendmedizin, Alexandrinenstrasse 5
      • Essen, Germany, 45147
        • Universitätsklinikum Essen, Klinik für Kinderheilkunde III, Pädiatrische Pneumologie und Schlafmedizin, Hufelandstr. 55
      • Essen, Germany, 45239
        • Ruhrlandklinik Essen, Westdeutsches Lungenzentrum am Universitätsklinikum Essen, Tuschener Weg 40

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

6 years and older (ADULT, OLDER_ADULT, CHILD)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Confirmed diagnosis of CF
  • Informed consent

Exclusion Criteria:

  • Cardiac arrhythmias with exercise
  • Patients with cor pulmonale
  • Colonization with Burkholderia cenocepacia, Methicillin-resistant Staphylococcus aureus (MRSA) and multidrug-resistant Gram-negative (MRGN) pathogens (3 and 4 MRGN)
  • Patients with untreated diabetes

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: TREATMENT
  • Allocation: NON_RANDOMIZED
  • Interventional Model: PARALLEL
  • Masking: NONE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
EXPERIMENTAL: Exercise Group
  1. First 6 months supervised exercise program with telephone contact every two weeks
  2. Second 6 months exercise program without telephone contact
  3. Patients should increase habitual daily physical activity for 10-20 minutes per day 5 times per week
  4. Activities were chosen according to the preferences, interests, and severity of disease of the patients
  5. Activites should improve endurance, strength, coordination and flexibility
  6. Every three month regular vistit at the CF care center (medical examination, lung function, exercise testing, counselling and evaluation of activities by acceleometry and if appropirate adaption of exercise program)
The exercise program is planned as a "low-threshold exercise program "with low barriers to participate. Patients will be asked about their interests and preferences of sports activities to conceive the exercise program together with the patients.
NO_INTERVENTION: Control-Group
  1. 12 months usual routine care and habitual exercise in daily life.
  2. At start and after 12 month assessment of habitual exercise with accelerometry (Actigraph GTX3)

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change of habitual physical activity in hours/day
Time Frame: at baseline, after 6 and 12 month
Measurement of the time of physical activity in hours/day by accelerometry (ActiGraph GT3X, Penascola, USA)
at baseline, after 6 and 12 month

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change of the quality of life in Cystic Fibrosis
Time Frame: at baseline, after 6 and 12 month
Measurement of the quality of life by the Cystic Fibrosis Questionnaire Revised (CFQ-R, Quality of life domains: Physical, role/school, vitality, emotion, social, body image, eating, treatment burden, health perceptions. Symptom scales: Weight, respiratory, and digestion)
at baseline, after 6 and 12 month
Change of the duration of sleep in hours
Time Frame: at baseline, after 6 and 12 month
Measurement of the duration of sleep in hours by accelerometry (ActiGraph GT3X, Penascola, USA)
at baseline, after 6 and 12 month
Change of the quality of sleep in percent
Time Frame: at baseline, after 6 and 12 month
Measurement of the quality of sleep in percent by accelerometry (ActiGraph GT3X, Penascola, USA)
at baseline, after 6 and 12 month
Determination of the exercise related barriers and barrier management in physical exercise
Time Frame: at baseline
specific questionnaire (Barrieren und Barrierenmanagementim Prozess der Sportteilnahme, Krämer and Fuchs, Zeitschrift für Gesundheitspsychologie, 18(4), 170-182, 2010)
at baseline
Change of habitual physical activity in steps/day
Time Frame: at baseline, after 6 and 12 month
Measurement of the number of steps/day by accelerometry (ActiGraph GT3X, Penascola, USA)
at baseline, after 6 and 12 month
Change of habitual physical activity spend in light intensity (≤ 3METS) in minutes
Time Frame: at baseline, after 6 and 12 month
Measurement of the time of habitual physical activity spend in light intensity (≤ 3METS) in minutes by accelerometry (ActiGraph GT3X, Penascola, USA)
at baseline, after 6 and 12 month
Change of habitual physical activity spend in moderate to vigorous intensity (3 to 5.9 METS) in minutes by accelerometry (ActiGraph GT3X, Penascola, USA)
Time Frame: at baseline, after 6 and 12 month
Measurement of the time of habitual physical activity spend in moderate to vigorous intensity (3 to 5.9 METS) in minutes by accelerometry (ActiGraph GT3X, Penascola, USA)
at baseline, after 6 and 12 month
Change of habitual physical activity spend in vigorous intensity (6 to 8.99 METS) in minutes by accelerometry (ActiGraph GT3X, Penascola, USA)
Time Frame: at baseline, after 6 and 12 month
Measurement of the time of habitual physical activity spend in vigorous intensity (6 to 8.99 METS) in minutes by accelerometry (ActiGraph GT3X, Penascola, USA)
at baseline, after 6 and 12 month
Change of habitual physical activity spend in hard intensity (≥ 9 METS) in minutes by accelerometry (ActiGraph GT3X, Penascola, USA)
Time Frame: at baseline, after 6 and 12 month
Measurement of the time of habitual physical activity spend in hard intensity (≥ 9 METS) in minutes by accelerometry (ActiGraph GT3X, Penascola, USA)
at baseline, after 6 and 12 month
Change of maximal exercise capacity expressed as heart rate
Time Frame: at baseline, after 6 and 12 month
Measurement of heart rate in b/min by cycle ergometry (Ergoselect 100p, Ergoline, Bitz, Germany)
at baseline, after 6 and 12 month
Change of maximal exercise capacity expressed as heart rate reserve in percent
Time Frame: at baseline, after 6 and 12 month
Measurement of heart rate reserve in percent by cycle ergometry (Ergoselect 100p, Ergoline, Bitz, Germany)
at baseline, after 6 and 12 month
Change of maximal exercise capacity expressed as workload in Watt
Time Frame: at baseline, after 6 and 12 month
Measurement of workload in Watt by cycle ergometry (Ergoselect 100p, Ergoline, Bitz, Germany)
at baseline, after 6 and 12 month
Change of maximal exercise capacity expressed as workload in Watt / kg bodyweight
Time Frame: at baseline, after 6 and 12 month
Measurement of workload in Watt / kg bodyweight by cycle ergometry (Ergoselect 100p, Ergoline, Bitz, Germany)
at baseline, after 6 and 12 month
Change of maximal exercise capacity expressed as perceived exertion (Borg CR10 Scale) in number of level of exertion
Time Frame: at baseline, after 6 and 12 month
Measurement of the Borg questionnaire (Borg CR10 Scale)
at baseline, after 6 and 12 month
Change of skill / performance related fitness expressed as push-ups in number of repetition in 40 sec.
Time Frame: at baseline, after 6 and 12 month
Measurement of push-ups in number of repetition in 40 sec. with the German motor test (Deutscher Motorik Test, Forschungszentrum für den Schulsport und den Sport von Kindern und Jugendlichen, Karlsruhe, Germany) in children and adolescents aged 6-18 years
at baseline, after 6 and 12 month
Change of skill / performance related fitness expressed as standing broad jump in cm in children and adolescents
Time Frame: at baseline, after 6 and 12 month
Measurement of standing broad jump in cm with the German motor test (Deutscher Motorik Test, Forschungszentrum für den Schulsport und den Sport von Kindern und Jugendlichen, Karlsruhe, Germany) aged 6-18 years
at baseline, after 6 and 12 month
Change of skill / performance related fitness expressed as sit-up in number of repetition in 40 sec.
Time Frame: at baseline, after 6 and 12 month
Measurement of sit-ups in number of repetition in 40 sec. with the German motor test (Deutscher Motorik Test, Forschungszentrum für den Schulsport und den Sport von Kindern und Jugendlichen, Karlsruhe, Germany) aged 6-18 years
at baseline, after 6 and 12 month
Change of skill / performance related fitness expressed as balancing backwards number in steps on a wooden beam 6 cm wide and 3 meters long
Time Frame: at baseline, after 6 and 12 month
Measurement of balancing backwards number in steps on a wooden beam 6 cm wide and 3 meters long with the German motor test (Deutscher Motorik Test, Forschungszentrum für den Schulsport und den Sport von Kindern und Jugendlichen, Karlsruhe, Germany) aged 6-18 years
at baseline, after 6 and 12 month
Change of skill / performance related fitness expressed as jump sideways in number of repetition in 15 sec.
Time Frame: at baseline, after 6 and 12 month
Measurement of balancing backwards number in jump sideways in number of repetition in 15 sec. with the German motor test (Deutscher Motorik Test, Forschungszentrum für den Schulsport und den Sport von Kindern und Jugendlichen, Karlsruhe, Germany) aged 6-18 years
at baseline, after 6 and 12 month
Change of skill / performance related fitness expressed as flexibility in cm in children and adolescents
Time Frame: at baseline, after 6 and 12 month
Measurement of flexibility in cm with the German motor test (Deutscher Motorik Test, Forschungszentrum für den Schulsport und den Sport von Kindern und Jugendlichen, Karlsruhe, Germany) aged 6-18 years
at baseline, after 6 and 12 month
Change of skill / performance related fitness expressed as one leg stand in sec.
Time Frame: at baseline, after 6 and 12 month
Measurement of one leg stand in sec. as included in the TFR (Test Fitness Rekrutierung, Bundesamt für Sport BASPO, Magglingen, Schweiz) in adults
at baseline, after 6 and 12 month
Change of skill / performance related fitness expressed as standing broad jump in cm in adults
Time Frame: at baseline, after 6 and 12 month
Measurement of standing broad jump in cm as included in the TFR (Test Fitness Rekrutierung, Bundesamt für Sport BASPO, Magglingen, Schweiz) in adults
at baseline, after 6 and 12 month
Change of skill / performance related fitness expressed as trunk power in sec.
Time Frame: at baseline, after 6 and 12 month
Measurement of trunk power in sec. as included in the TFR (Test Fitness Rekrutierung, Bundesamt für Sport BASPO, Magglingen, Schweiz) in adults
at baseline, after 6 and 12 month
Change of skill / performance related fitness expressed as flexibility in cm in adults
Time Frame: at baseline, after 6 and 12 month
Measurement of flexibility in cm as included in the basic motor diagnostics (Motorische Basisdiagnostik, Hrsg. Bös/Wydra/Karisch, 1992) in adults
at baseline, after 6 and 12 month
Change of skill / performance related fitness expressed as circling motion in number of complete performed circles
Time Frame: at baseline, after 6 and 12 month
Measurement of circling motion in number of complete performed circles as included in the basic motor diagnostics (Motorische Basisdiagnostik, Hrsg. Bös/Wydra/Karisch, 1992) in adults
at baseline, after 6 and 12 month
Change of skill / performance related fitness expressed as the time of hip extension in sec.
Time Frame: at baseline, after 6 and 12 month
Measurement of the time of hip extension in sec. as included in the basic motor diagnostics (Motorische Basisdiagnostik, Hrsg. Bös/Wydra/Karisch, 1992) in adults
at baseline, after 6 and 12 month

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

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Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (ACTUAL)

September 10, 2014

Primary Completion (ACTUAL)

August 10, 2018

Study Completion (ACTUAL)

August 10, 2018

Study Registration Dates

First Submitted

March 26, 2018

First Submitted That Met QC Criteria

May 7, 2018

First Posted (ACTUAL)

May 8, 2018

Study Record Updates

Last Update Posted (ACTUAL)

January 3, 2019

Last Update Submitted That Met QC Criteria

January 2, 2019

Last Verified

January 1, 2019

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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