Universitaire Ziekenhuizen Leuven, campus Pellenberg
Pellenberg, 3212, Belgium
NCT Number: NCT03109483
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.
Looking for future studies?
Notify Me70 year and older
All sexes
Interventional
Not applicable
Pellenberg, 3212, Belgium
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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
intensive multicomponent physical therapy week program
Time frame: four weeks
Independence for ADL measured with the Basic-ADL
Time frame: four weeks
Functional balance measured with the Berg Balance Scale
Time frame: four weeks
Walking speed measured with the 10m walking test
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.
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.
Time frame: four weeks
The Digit Symbol Substitution Test will be used to measure response speed, sustained attention
Time frame: four weeks
General state of mind measured with the Geriatric Depression Scale 15
KU Leuven
Other
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT04865627
Abdominal Injuries, Abdominal Injury
Leuven, Belgium
View Trial DetailsNCT02425345
Arterial Occlusive Diseases, Arteriosclerosis
View Trial DetailsNCT04141891
Acute Coronary Syndrome, Aortic Stenosis, Subvalvular
La Jolla, California, United States
View Trial DetailsNCT02232126
Asthma, Behavior
Los Angeles, California, United States
View Trial Details