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Clinical Trials/NCT04207307
NCT04207307
Completed
Not Applicable

Best Function of Range of Motion (cRCT)

Technical University of Munich1 site in 1 country404 target enrollmentNovember 3, 2020
ConditionsMobility

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Mobility
Sponsor
Technical University of Munich
Enrollment
404
Locations
1
Primary Endpoint
Change in Short Physical Performance Battery
Status
Completed
Last Updated
4 months ago

Overview

Brief Summary

Mobility is a crucial factor for independence and quality of life in older people. However, the majority of those in retirement homes are not physically active to maintain mobility and independence.

The aim of the cluster randomized controlled bestform trial in 20 retirement homes (1:1 randomization) is to evaluate the efficacy of a multimodal exercise program for older people living in retirement homes in comparison to usual care over 6 months.

Within the intervention facilities, the participants will take part in a physical activity program over 6 months (2 times a week à 45 min) consisting of machine-based strength, coordination and endurance training.

Criteria of effectiveness are changes in physical function (primary endpoint: Change of Short Physical Performance Battery Score after 6 months) and the following secondary endpoints: mobility and balance, rate of falls, cardiometabolic risk factors, myocard function, quality of life and lifestyle factors (nutrition, physical activity), assessed by medical assessments, physical performance tests and various questionnaires after 3 and 6 months. Follow-up data will be collected after 18 and 30 months (questionnaire).

Detailed Description

Mobility is a crucial factor for independence and quality of life at old age. Particularly those in retirement homes have a reduced physical activity status. The aim of the bestform trial is the integration of an exercise concept comprising resistance, coordination and endurance training in retirement homes to promote mobility and independence as well as to reduce the risk of falling in older people. The study is organized and conducted as a multi-center, two-armed cluster randomized study in 20 retirement homes (1:1 randomization in intervention retirement homes and control retirement homes with usual care) in the area of Munich, Germany. A total of at least 400 older people will subsequently be recruited. It is expected to recruit n≥20 older people per participating retirement home. The intervention group will participate in an exercise training for 6 months, which will take place in the period from March 2020 to October 2021 (extended until August 2023). The multimodal intervention consists of a machine-based resistance, coordination and endurance training, which is performed 1-2 times per week for 30-45 minutes with increasing amount of training. Age and disability adapted pneumatic resistance training machines are used targeting large muscle groups. The endurance training is performed on upright-bicycle and recumbent bicycle ergometers. Coordination is exercised statically on the floor or a balance pad and dynamically on a balance-platform according to the individual training plan. The aim of the bestform trial is to examine the efficacy of this multimodal training on physical function measured by the Short Physical Performance Battery (SPPB) (primary endpoint) over a 6-month period. In addition, the impact of the training on mobility and balance, physical capacity (6-min-walk test), rate of falls, anthropometric parameters, cardiometabolic risk parameters (echocardiography, blood parameters), fear of falling, quality of life and other life style factors (nutrition, physical activity) assessed by medical assessments, physical performance tests and various questionnaires will be investigated after 3 and 6 months. Follow-up data will be collected after 18 and 30 months (questionnaire).

Registry
clinicaltrials.gov
Start Date
November 3, 2020
End Date
August 12, 2025
Last Updated
4 months ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Technical University of Munich
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Study participant must be resident of one of the participating retirement homes
  • Written informed consent of the study participant or legal representative
  • Being able to stand independently (without assistance)

Exclusion Criteria

  • Any acute or chronic illness or physical/mental condition as well as any form of dementia, which does not allow to stand independently or which does not allow physical training in small groups or which would require a training with medical supervision

Outcomes

Primary Outcomes

Change in Short Physical Performance Battery

Time Frame: Baseline to 6 months

The Short Physical Performance Battery is a summary performance score out of 3 tests (standing balance test, gait speed test, and chair-stand-test). Categories of performance will be formed for each performance test (0 points to 4 points) and a summary score will be used. The sum score ranges from 0 (worst performance) to 12 (best performance).

Secondary Outcomes

  • Change in body composition(Change after 3 and 6 months)
  • Change in calf circumference(Change after 3 and 6 months)
  • Change in balance ability and mobility(Change after 3 and 6 months)
  • Change in nutritional status(Change after 3 and 6 months)
  • Change in activity of daily living(Change after 3 and 6 months)
  • Change in handgrip strength(Change after 3 and 6 months)
  • Rate of falls(6 months)
  • Change in cardiac function(Change after 6 months)
  • Change in fear of falling(Change after 3 and 6 months)
  • Change in physical capacity(Change after 3 and 6 months)
  • Change in body weight(Change after 3 and 6 months)
  • Change in brain-derived neutrophic factor(Change after 3 and 6 months)
  • Change in risk for sarcopenia(Change after 3 and 6 months)
  • Change in Short Physical Performance Battery(Baseline to 3 months)
  • Change in inflammatory marker(Change after 3 and 6 months)
  • Change in cognition(Change after 6 months)
  • Change in quality of life(Change after 3 and 6 months)
  • Follow-up evaluation of MACE(Changes over 18 and 30 months)

Study Sites (1)

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