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Clinical Trials/NCT01371097
NCT01371097
Completed
Not Applicable

The Effect of Progressive Resistance Strength Training in Hospitalised Elderly Patients

Glostrup University Hospital, Copenhagen1 site in 1 country71 target enrollmentSeptember 2006

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Medical Diseases
Sponsor
Glostrup University Hospital, Copenhagen
Enrollment
71
Locations
1
Primary Endpoint
Timed "Up & Go" Test
Status
Completed
Last Updated
11 years ago

Overview

Brief Summary

The aim of the study is to evaluate the effect of progressive resistance strength training (PRT) in elderly hospitalised patients. The hypothesis is that PRT given as an additional training would improve the rehabilitation and increase the level of activity of daily living.

Detailed Description

Elderly inpatients included in the study were randomised into a control group or a training group. All included patients received the regular in-physiotherapy, but the training group received progressive resistance training in groups in addition.

Registry
clinicaltrials.gov
Start Date
September 2006
End Date
January 2008
Last Updated
11 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Glostrup University Hospital, Copenhagen
Responsible Party
Principal Investigator
Principal Investigator

Sigrid Tibaek

Dr Med Sci, pt

Glostrup University Hospital, Copenhagen

Eligibility Criteria

Inclusion Criteria

  • Hospitalised elderly patients referred for physiotherapy.
  • Ability to perform standing position independently with/without walking aids (rollator, crutch) or bed/bench support.

Exclusion Criteria

  • Expected length of stay \< 7 days.
  • Unable to communicate relevant.
  • Unable to be active

Outcomes

Primary Outcomes

Timed "Up & Go" Test

Time Frame: Before randomisation and 3 days before discharge from the department

The Timed Up \& Go (TUG) test assess basic functional mobility.(14). The test measures the time (in seconds)that the subjects used for standing up from the seating position on a chair (chair seat height = 45 cm) with armrest, walking 3 m, turning around and walking back to the chair and sitting down again.

Secondary Outcomes

  • Barthel Index(before randomisation and 3 days before discharge from the department)

Study Sites (1)

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