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CompletedNCT01371097B15Updated Mar 11, 2015

Progressive Resistance Strength Training (PRT) in Hospitalised Elderly Patients

An interventional study of Progressive Resistance strength training in Medical Diseases, Neurological Diseases and Chronical Obstructive Lung Diseases, sponsored by Glostrup University Hospital, Copenhagen. Completed at 1 site in Denmark. Open to participants aged 60 Years and older. Per ClinicalTrials.gov, last updated 2015-03-11.

Sponsored by Glostrup University Hospital, Copenhagen · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
71
Allocation
Randomized
Ages
60 Years and older
Sex
All
01

Study 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.

Read the 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.

02

Conditions studied

  • Medical Diseases
  • Neurological Diseases
  • Chronical Obstructive Lung Diseases

Keywords

  • Barthel Index
  • elderly hospitalised patients
  • progressive resistance training
03

In context

Lung Diseases

3,303 studies on the registry are indexed under Lung Diseases; 355 are open to participants now.

This study's enrollment of 71 is close to the median of 72 across 2,118 interventional studies indexed under Lung Diseases.

Browse Lung Diseases studies →

Lead sponsor

Glostrup University Hospital, Copenhagen is the lead sponsor of 104 studies on the registry; 5 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
60 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

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

Exclusion criteria

Exclusion Criteria:

  1. Expected length of stay \< 7 days.
  2. Dementia.
  3. Unable to communicate relevant.
  4. Unable to be active
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
71 participants (actual)

Study arms

  • No intervention
    Control Group
  • Experimental
    Treatment group

    Other: Progressive Resistance strength training

Interventions

  • OtherProgressive Resistance strength training

    Resistance strength training is given as circle training. The resistance is increased with regularly intervals.

06

What researchers measure

Primary outcomes

  1. Timed "Up & Go" Test

    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.

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

Secondary outcomes

  1. Barthel Index

    BI consists of 10 functional tasks of which 3 tasks focus the function of mowing and walking. Task numbers 8 in BI "Transfer" assess the ability to move and are rated on a 0, 5 and10 point ordinal scale. Task number 9 in BI "Walking" assess the ability to walk rated on a 0, 5 or 10 point scale. Task number 10 in BI "Stairs" assesses the ability to walk on stairs and is rated with 0, 5, 10 or 15 points.

    Time frame: before randomisation and 3 days before discharge from the department

07

Study locations

1 site
  • Copenhagen University Hospital, Glostrup
    Glostrup, DK-2600, Denmark
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 11, 2015, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01371097
Lead sponsor
Glostrup University Hospital, Copenhagen
Responsible party
Sigrid Tibaek (Dr Med Sci, pt, Glostrup University Hospital, Copenhagen) — Principal investigator
First posted
Jun 10, 2011
Start date
Sep 2006
Primary completion
Jan 2008
Completion
Jan 2008
Last update
Mar 11, 2015

Study contacts

Sigrid Tibaek, Dr Med Sci, PT
principal investigator · Copenhagen University Hospital, Glostrup

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Mar 2015. You cannot join it, but the record below documents what was studied.

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