- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02315963
Feedback and Rewards to Increase Motivation for Therapy in Stroke Rehabilitation
Study Overview
Detailed Description
High motivation is a predictor for good therapy results in physical therapy [Grahn 2000]. Additional focus on motivation and rewards has fallen on the topic of stroke rehabilitation since it was shown in an animal model that the brain centers involved with motivation and rewards are crucial to motor learning [Hosp 2011].
The investigators goal is to target the overall motivation for therapy. During the guided therapy sessions the therapists will be the main motivators and the investigators do not want to interfere with that. But the amount of guided therapy sessions is often limited due to economical reason rather than therapeutic ones. Therefore patients are encouraged to do training on their own if possible and to be active during the patients stay in the rehabilitation clinic. The investigators target the patients motivation to train by themselves and be active but also the patients attitude towards the guided therapies. It is known that performance feedback can improve motivation [Harackiewicz 1979]. Therefore the investigators want to use the data about therapy progress to produce feedback for patients visualizing the patients progress and efforts during the patients stay in the clinic.
The investigators will compare patients who receive normal therapy to patients who receive normal therapy plus performance feedback regarding a variety of motivation measures.
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Lucerne
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Vitznau, Lucerne, Switzerland, 6354
- Cereneo, Center For Rehabilitation and Neurology
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- First time Inpatient at the Cereneo rehabilitation clinic
Exclusion Criteria:
- Rey-Figur Kopie <= 25 AND Rechnerisches Denken WIE <=5
- Becks Depression Inventar (BDI) > 17
- Major aphasia preventing understanding of study materials (according to the treating physician).
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
No Intervention: No intervention group
Patients in stroke rehabilitation receiving standard therapy
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Active Comparator: Intervention group
Patients in stroke rehabilitation receiving standard therapy plus performance feedback
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Performance Feedback regarding the patients efforts and accomplishments during the patients stay in the rehabilitation clinic, an expected average of 6 weeks.
The data available about the patients progress will be analysed and processed to create a visual illustration shown to the patient on a daily bases.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Motivation
Time Frame: Weekly for the duration of the participants stay at the hospital an expected average of 6 weeks
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Weekly: Intrinsic Motivation Inventory Questionnaire
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Weekly for the duration of the participants stay at the hospital an expected average of 6 weeks
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Motivation
Time Frame: After each therapy session for the duration of the participants stay at the hospital an expected average of 6 weeks
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Motivation rating of patients regarding the foregoing therapy session by therapists
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After each therapy session for the duration of the participants stay at the hospital an expected average of 6 weeks
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Motivation
Time Frame: Continuous for the duration of the participants stay at the hospital an expected average of 6 weeks
|
Time patient spends on self administered training
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Continuous for the duration of the participants stay at the hospital an expected average of 6 weeks
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Motivation
Time Frame: Continuousfor the duration of the participants stay at the hospital an expected average of 6 weeks
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Amount of activities (walking, stair climbing) during free time
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Continuousfor the duration of the participants stay at the hospital an expected average of 6 weeks
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Clinical scores (e.g. Fugl-Meyer Score)
Time Frame: When decided by therapists for the duration of the participants stay at the hospital an expected average of 6 weeks
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Standard quality assessments of the study site (rehabilitation clinic)
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When decided by therapists for the duration of the participants stay at the hospital an expected average of 6 weeks
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Collaborators and Investigators
Sponsor
Publications and helpful links
General Publications
- Grahn B, Ekdahl C, Borgquist L. Motivation as a predictor of changes in quality of life and working ability in multidisciplinary rehabilitation. A two-year follow-up of a prospective controlled study in patients with prolonged musculoskeletal disorders. Disabil Rehabil. 2000 Oct 15;22(15):639-54. doi: 10.1080/096382800445443.
- Hosp JA, Pekanovic A, Rioult-Pedotti MS, Luft AR. Dopaminergic projections from midbrain to primary motor cortex mediate motor skill learning. J Neurosci. 2011 Feb 16;31(7):2481-7. doi: 10.1523/JNEUROSCI.5411-10.2011.
- Harackiewicz, Judith M. The effects of reward contingency and performance feedback on intrinsic motivation. Journal of Personality and Social Psychology, Vol 37(8), Aug 1979, 1352-1363.
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
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
- KFSP Feedback Study
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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