- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03997591
Upper Limb Reeducation Across Life Span (ULReed)
Effect of Ready2E.A.T. in Risk Populations
Program Ready2E.A.T. was developed to be tested in the upper limb reeducation on population at risk, such as:
- Children with dysfunction
- Cognitive impaired elderly
- Dementia people
Study Overview
Status
Intervention / Treatment
Detailed Description
Program Ready2E.A.T. consists on the training of specific upper limb tasks, including:
- reaching during attention tasks
- reaching during memory tasks
- reaching during sequential motor tasks
- reaching during fine hand movements
This program has been tested as a measure of functional status (cognitive and motor habilities) in population with different risks; It also has been tested as an effective program for reeducation in cognitive affected population.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
-
Leiria, Portugal
- Instituto Politécnico de Leiria
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- people with 60years old with cognitive decline
- children aging 6-10 years old with cognitive and motor dysfunction
- dysfunction in feeding participation
Exclusion Criteria:
- participants that do not understand 2 simnultaneous verbal commands
Study Plan
How is the study designed?
Design Details
- Observational Models: Case-Control
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Conventional therapy
Group doing conventional rehabilitation was assessed at T0 and then after 6 weeks of conventional therapy (occupational therapy, physical therapy, aquatic therapy, musicotherapy, others)
|
Training tasks based on: reaching activities during attention tasks, memory tasks, sequential tasks This group was assessed at T0 and then after 6 weeks of conventional therapy. |
Ready2E.A.T. therapy
Group doing Ready2E.A.T. program received a mean of 1 hour per week and was assessed at T0 and then after 6 weeks of this program implementation.
|
Training tasks based on: reaching activities during attention tasks, memory tasks, sequential tasks This group was assessed at T0 and then after 6 weeks of conventional therapy. |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Video analysis of feeding performance
Time Frame: 6 weeks
|
performance of several feeding steps
|
6 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Frontal assessment battery
Time Frame: 6 weeks
|
Assessment of Executive Functions
|
6 weeks
|
Collaborators and Investigators
Sponsor
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
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- IPL10062019
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
product manufactured in and exported from the U.S.
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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