- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03754478
Follow-Up of Fitness in Overweight Patients Treated With Physical Activity (FUFPA)
Although there is increasing evidence that low physical fitness is a risk factor for many non-communicable diseases, the early identification of subjects at risk remains inadequate due to the absence of clear anamnestic and clinical criteria. Defining physical fitness. For the same reason, the monitoring of subjects following lifestyle interventions remains suboptimal.
The aim of this study is to develop a simple field tool to non-invasively assess global physical fitness in overweight patients participating to a physical activity program.
Male and female overweight subjects referred to a physical activity intervention by their primary care physician will be included. Within this program, they will take part to 2 weekly supervised activity sessions during which participants will be instructed by a specialist in adapted physical activity, and 2-3 weekly session of unsupervised physical activity which will be performed according to detailed instructions regarding intensity and duration. In addition, participants will take part to teaching sessions in group of 4-6 patients, addressing the effects of physical activity on metabolism, contra-indications to physical activity, self-monitoring of exercise, and prevention of injuries Their physical fitness will be assessed at inclusion (ie before starting the exercise program) and at the end of the 3-month program. This will be done by calculating a Global Fitness Score (GFS) based on performances attained and cardiovascular responses observed during physical exercises (3 min step test with measurement of heart rate and blood pressure, number of time subject can stand from a chair within 1 min., handgrip strength measure, "reach-test" to assess osteo-articular mobility of back and hips, balance test). Results obtained from this GFS will be compared to maximal power output calculated from a submaximal spirometry at 25, 50, 75 and 100 W M.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Sedentarity is a risk factor for overweight, insulin resistance and diabetes mellitus. Several randomized clinical trials have shown that lifestyle interventions including exercise are efficient in improving metabolic homeostasis in overweight and obese patients. This may be related sedentarity being associated with low physical fitness, and to training enhancing it through multiple systems effects (cardiovascular and respiratory systems, central nervous system, osteo-articular system).
Although there is increasing evidence that low physical fitness is a risk factor for many non-communicable diseases, the early identification of subjects at risk remains inadequate due to the absence of clear anamnestic and clinical criteria. Defining physical fitness. For the same reason, the monitoring of subjects following lifestyle interventions remains suboptimal.
The aim of this study is to develop a simple field tool to non-invasively assess global physical fitness in overweight patients participating to a physical activity program.
Eigtheen male and female subjects, aged 18-50 years, BMI >27 kg/m2 referred to a physical activity intervention by their primary care physician, will be included. Their physical fitness will be assessed at inclusion (ie before starting the exercise program) and at the end of the 3-month program.This will be done by calculating a Global Fitness Score (GFS) based on performances attained and cardiovascular responses observed during 5 physical exercises (3 min step test with measurement of heart rate and blood pressure, number of time subject can stand from a chair within 1 min., handgrip strength measure, "reach-test" to assess osteo-articular mobility of back and hips, balance test). Results obtained from this GFS will be compared to maximal power output calculated from a submaximal spirometry at 25, 50, 75 and 100 W Primary outcome are: GFS (composite of a score of physical endurance, two scores of muscle strength, one score of balance, and one score of osteo-articular mobility) before and after 3 months of intervention.
Secondary outcomes are: physical activity questionnaire, maximal power output; maximal oxygen consumption; fat oxidation; fasting metabolic profile before and after 3 months of intervention.
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Locations
-
-
Fribourg
-
Estavayer le lac, Fribourg, Switzerland, 1470
- Recruiting
- Hôpital Intercantonal de la Broye
-
Contact:
- Virgile Lecoultre, PhD
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- BMI >27 kg/m2
Exclusion Criteria:
- cardio-respiratory diseases
- severe osteo-articular diseases
- any condition associated with contra-indication to exercise.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
overweight subjects
Overweight male and females referred to a physical activity program by their primary care physician Intervention is being included in a 3-month physical activity training program
|
subjects will enter a 3-month supervised physical activity program during which they will take part to supervised and unsupervised physical activity sessions.
Type of physical activity will be selected among a number of available activities (aquagym, aerobics, resistance training, outdoors activities) based on individual needs and preferences); it will consist in 2 weekly supervised activity sessions during which participants will be instructed by a specialist in adapted physical activity, and 2-3 weekly session of unsupervised physical activity which will be performed according to detailed instructions regarding intensity and duration.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in Global Fitness Score before and after 3 months physical training
Time Frame: After 3 month physical training
|
Global fitness score ranges between 0 (very low fitness) and 30 (optimal fitness).
It is calculated as the sum of scores obtained with 5 simple field tests (Chester step test, score 0-10; handgrip, score 0-5; sit-and stand test, score 0-5; Sit and reach test, score 0-5; Flamingo test, score 0-5)
|
After 3 month physical training
|
Collaborators and Investigators
Sponsor
Investigators
- Study Chair: Charly Bulliard, MD, Hopital Intercantonal de la Broye, Estavayer le-lac, Switzerland
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2018-00147
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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.
Clinical Trials on Exercise Training
-
Adiyaman UniversityActive, not recruitingHigh-Intensity Interval Training | Exercise Physiology | Exercise Training AdaptationTurkey (Türkiye)
-
Hamza KucukCompletedExercise Training | Exercise PhysiologyTurkey (Türkiye)
-
University of British ColumbiaMOSS ROCK PARK FOUNDATIONNot yet recruiting
-
Universiti Putra MalaysiaEnrolling by invitation
-
University of NebraskaCompletedExercise TrainingUnited States
-
University of CalgaryNatural Sciences and Engineering Research Council, CanadaCompleted
-
University of TorontoCompleted
-
University of Southern CaliforniaCompleted
-
Universitaire Ziekenhuizen KU LeuvenCompleted
Clinical Trials on Physical activity training
-
Enes SucularCompleted
-
Federal University of São PauloUnknownSystemic Lupus ErythematosusBrazil
-
University of Sao Paulo General HospitalFundação de Amparo à Pesquisa do Estado de São PauloCompletedPlatelet Aggregation | Exercise Training | Acute Myocardial InfarctionBrazil
-
Tel Aviv UniversityHerzliya Medical CenterRecruitingObesity | Adiposity | Muscle LossIsrael
-
Büşra SOLMAZ AYDINActive, not recruitingQuality of Life | Health Promotion | Healthy Lifestyle | Physical FitnessTurkey (Türkiye)
-
Assistance Publique Hopitaux De MarseilleCompletedPediatric CancerFrance
-
Fondazione Policlinico Universitario Agostino Gemelli...TerminatedParkinson DiseaseItaly
-
Assaf-Harofeh Medical CenterBen-Gurion University of the NegevUnknown
-
Centre Hospitalier Universitaire de NiceRecruitingObesity | Bariatric Surgery CandidateFrance
-
Northwestern UniversityCompletedSedentary BehaviorUnited States