- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02235922
Effects of a Dual Task Protocol on Cognition and Functionality in Non-sedentary Older Adults
September 6, 2014 updated by: Anielle C M Takahashi, Universidade Federal de Sao Carlos
The purpose of this study is to analyze the effects of a dual task protocol on cognitive domains and functional capacity in non-sedentary older adults.
The hypothesis of the present study is that older people undergoing to a dual task exercise protocol have greater benefits on cognition and functional performance, compared to a standard exercise protocol.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
78
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
São Paulo
-
São Carlos, São Paulo, Brazil, 13565-905
- Universidade Federal de Sao Carlos
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
60 years to 90 years (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- aged over 60 years
- community people
- ability to walk alone
- non-sedentary
Exclusion Criteria:
- non-realization of any cognitive or functional assessment
- presence of Parkinson's Disease, Dementia and Stroke with motor sequel
- frequency to trainings below 70%
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Dual task training
|
The dual task training consisted of individuals subjected to a multicomponent exercise program associated to cognitive tasks.
|
Experimental: Conventional training
|
The conventional training consisted of individuals subjected to a multicomponent exercise program.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Changes on cognition after 3 months of training
Time Frame: Assessed at baseline and after 3 months of training
|
Cognition was assessed by Montreal Cognitive Assessment and Mini-Mental State Examination
|
Assessed at baseline and after 3 months of training
|
Changes on functional capacity after 3 months of training
Time Frame: Assessed at baseline and after 3 months of training
|
Functional capacity was assessed by Timed up and go test, Timed up and go test associated to a cognitive task and sit to stand test.
|
Assessed at baseline and after 3 months of training
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Anielle Takahashi, doctorate, Universidade Federal de Sao Carlos
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
March 1, 2014
Primary Completion (Actual)
August 1, 2014
Study Registration Dates
First Submitted
September 6, 2014
First Submitted That Met QC Criteria
September 6, 2014
First Posted (Estimate)
September 10, 2014
Study Record Updates
Last Update Posted (Estimate)
September 10, 2014
Last Update Submitted That Met QC Criteria
September 6, 2014
Last Verified
September 1, 2014
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- LAPESI-01
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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