Skip to main content
Clinical Trials/NCT00877721
NCT00877721
Completed
Not Applicable

Self Mobility Improvement in the Elderly by Counteracting Falls (SMILING)

Soroka University Medical Center1 site in 1 country30 target enrollmentApril 2010
ConditionsFalls

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Falls
Sponsor
Soroka University Medical Center
Enrollment
30
Locations
1
Primary Endpoint
gait analysis
Status
Completed
Last Updated
15 years ago

Overview

Brief Summary

Experimental design overview:

The proposed project is a prospective experimental study design. Independent old adults (age 65 years old and older) who suffer from minor balance problems willing to participate in the study will be tested with well-established measuring techniques of balance and gait before and 4 weeks after balance training program using the "Self Mobility Improvement in the Elderly by Counteracting Falls" system (SMILING system). The study design is randomized clinical trial (RCT), cross over, single blinded study design where 30 subjects will randomly be allocated into experimental or control groups that will switch groups after 4 weeks of intervention.

Random sequence generation will be performed by a staff member who will not interact with subjects during the balance-testing sessions. Subjects will be informed that they are to be randomly assigned to one of the two groups, both receiving gait training program.

The staff member who administers the training programs will be the only member of the research team aware of the subjects' group allocations.

A 'blinded' research assistant will administer the balance tests and will perform any data processing that involves subjective judgments.

Scripts will be used during testing to ensure that all subjects receive the same instructions.

Testing session between two training periods (T1) will take one week.

Registry
clinicaltrials.gov
Start Date
April 2010
End Date
July 2010
Last Updated
15 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

gait analysis

Time Frame: time 1: pre test; time 2 post test (4 weeks after pre test) and time 3 follow up (8 weeks after pre test)

Secondary Outcomes

  • Tinetti's performance-oriented mobility assessment (POMA score), CODEX test, GDS test(time 1: pre test; time 2 post test (4 weeks after pre test) and time 3 follow up (8 weeks after pre test))
  • CODEX test(time 1: pre test; time 2 post test (4 weeks after pre test) and time 3 follow up (8 weeks after pre test))
  • GDS test(time 1: pre test; time 2 post test (4 weeks after pre test) and time 3 follow up (8 weeks after pre test))

Study Sites (1)

Loading locations...

Similar Trials