- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02621697
Dual Task in Institutionalized Elderly
Dual Task in Institutionalized Elderly: Positive Impact on the Risk of Falls and Functionality
Objectives: To evaluate the effects of eight weeks of cognitive motor training (dual task) in the risk of falls, balance, independence in basic activities of daily living (BADL) and handgrip in institutionalized elderly.
Methods: The sample was divided in two groups: double task group (DTG), consists of five elderly, undergoing a training consists of motor and cognitive activities and control group (CG) consists of four seniors who underwent conventional kinesiotherapeutic training, based on global stretching and strengthening exercises, both held in 16 sessions.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion criteria:
- individuals over the age of 60,
- minimum score of 18 points on the Mini-Mental State Examination (MMSE),
- individuals classified as sedentary according the International Physical Activity Questionnaire (short version IPAQ-),
- literate and visual acuity preserved or corrected.
Exclusion criteria:
- Individuals unable to remain standing upright
- individuals dependent from auxiliary device to walk
- those who performed another type of physical therapy intervention concomitantly
Study Plan
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: Cognitive motor training
Evaluate the effectiveness of a 12-week training based on dual-task (motor and cognitive) in institutionalized elderly.
|
Initially an intervention consisting of double duty activities (motor-cognitive) and the control group will be subjected to a conventional treatment based on stretching and strengthening will be held.
|
|
Active Comparator: Control Group
kinesiotherapeutic conventional treatment
|
Standardized global stretching and strengthening with squat exercise, plantar flexion in foot and elbow flexion supporting body weight in the hands arranged on the wall
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Risk of falls
Time Frame: 8 weeks of training
|
Measured by the following tests: TUG, motor TUG, cognitive TUG, Romberg and sensitized Romberg (all measured in seconds)
|
8 weeks of training
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Independence to carry out basic activities of daily living
Time Frame: 8 weeks of training
|
Through the modified Katz scale: the simulation of the activities originally present in the Katz scale was performed by the participants, and the time taken to their execution was recorded.
|
8 weeks of training
|
|
Muscle strength
Time Frame: 8 weeks of training
|
Through dynamometry
|
8 weeks of training
|
Collaborators and Investigators
Investigators
- Principal Investigator: Lislei Patrizzi, Professor, Universidade Federal do Triangulo Mineiro
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 (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
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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