- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03109483
Effectiveness of the Geriatric Activation Program Pellenberg (GAPP) on the Geriatric Rehabilitation Ward
The aim of this study is to investigate the effectiveness of our developed week-treatment program GAPP, on strength, balance, speed, functionality and cognition, with the main goal to achieve a better independence for activities of daily living (ADL).
Each day of the week an exercise program of 45 minutes is given assigned to a specific aspect of the rehabilitation; strength, balance, speed, functional training and one day is for testing or group therapy.
Participants will be followed for four weeks, with testing on day one, after two weeks and at the last day of the four-week program.
Study Overview
Status
Intervention / Treatment
Detailed Description
The aim of this study is to investigate the effectiveness of our developed week-treatment program GAPP (Geriatric Activation Program Pellenberg), on strength, balance, speed, functionality and cognition, with the main goal to achieve a better independence for ADL.
Each day of the week an exercise program of 45 minutes is given assigned to a specific aspect of the rehabilitation.
Monday: speed and coordination, including as many repetitions as possible in one minute for: quick arm movements in standing, quick trunk movements in sitting, quick weight transfers in standing, stepping.
Tuesday: functional training, including walking stairs, transfers, sitting to lying and reverse, moving objects in the room, functional fit-o-meter.
Wednesday: balance, including maximum weight transfers in all directions, exercises with reduced base of support, reaching.
Thursday: strength, including sit to stand with a weight belt, lifting a weight bimanual of the table, walking with ankle weights, arm extension with therapy bands.
Friday: testing or group activity. One week the following test will be taken: Berg Balance Scale, 10m walking test, Digit Symbol Substitution Test, knee extension and elbow extension strength with the microfet2, Basic-ADL and Geriatric Depression Scale.
The other week there will be a group session, this could be in sitting (like moving on music) or standing (like petanque).
Walking will be practiced every day of the week and individual needs (like specific hand rehabilitation or pain problems) will be addressed besides the program when needed.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Pellenberg, Belgium, 3212
- Universitaire Ziekenhuizen Leuven, campus Pellenberg
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- admitted to the geriatric rehabilitation ward of UZ Leuven, campus Pellenberg
- the ability to walk 10m with help of a person or walking aid
- an expected stay of at least four weeks
- a signed informed consent
Exclusion Criteria:
- medically instable
- not able to understand the questions and tasks of the program or testing
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Other: Geriatric Activation Program Pellenberg
intensive multicomponent physical therapy week program
|
intensive multicomponent physical therapy week program
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Independence for activities of daily living
Time Frame: four weeks
|
Independence for ADL measured with the Basic-ADL
|
four weeks
|
|
Functional Balance
Time Frame: four weeks
|
Functional balance measured with the Berg Balance Scale
|
four weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Walking speed
Time Frame: four weeks
|
Walking speed measured with the 10m walking test
|
four weeks
|
|
Strength of arm Extension
Time Frame: four weeks
|
Strength of arm extension, measured with the microFET2 hand held dynamometer.
The mean peak force in Newton of three trail will be used.
|
four weeks
|
|
Strength of knee extension
Time Frame: four weeks
|
Strength of Knee extension, measured with the microFET2 hand held dynamometer.
The mean peak force in Newton of three trail will be used.
|
four weeks
|
|
Cognitive function
Time Frame: four weeks
|
The Digit Symbol Substitution Test will be used to measure response speed, sustained attention
|
four weeks
|
|
General state of mind
Time Frame: four weeks
|
General state of mind measured with the Geriatric Depression Scale 15
|
four weeks
|
Collaborators and Investigators
Sponsor
Collaborators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
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
- S59948 / B322201731432
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.
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