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

S

Soroka University Medical Center

Status

Completed

Conditions

Falls

Treatments

Device: Self Mobility Improvement in the eLderly by using the SMILING system

Study type

Interventional

Funder types

Other

Identifiers

NCT00877721
SOR483209CTIL
MZ4832

Details and patient eligibility

About

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.

Enrollment

30 patients

Sex

All

Ages

65+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

The inclusion criteria are:

Self-reported information

  1. age ≥ 65 years,
  2. able to walk at least 20 meters independently, i.e., without personal assistance and without an assistive device, except for a single point cane
  3. one or more falls in the previous year (falls during sport activities excluded).

Standardized physical and cognitive functional tests

  1. Tinetti's POMA score below 26 (strictly)
  2. MMSE test with score ≥ 24
  3. GDS test with score <10

The exclusion criteria are:

  1. Self-reported information
  2. age < 65 years
  3. inability to walk 20 meters safely (self-report) or walk with personal assistance or with an assistive device (except single point cane for fallers)
  4. inability to recall fall status in the previous year
  5. severe visual impairment (e.g., impaired ability to read, watch TV, or drive a car)
  6. severe hearing impairment (e.g., unable to follow a conversation, to use a phone)
  7. Standardized physical and cognitive functional tests
  8. Tinetti's POMA score less than 19
  9. MMSE score < 24
  10. GDS test with score ≥ 10
  11. Medical conditions (filled in by the family doctor of the subject)
  12. wearing a pacemaker, a cardiac defibrillator or any other electronic implant
  13. severe gait impairment precluding safe walking over 20 meters due to:
  14. focal lower limb muscle weakness or palsy (e.g., unable to raise leg/foot from floor)
  15. neurological diseases, including diseases such as severe Parkinson's disease, Multiple Sclerosis, status post stroke with hemi-syndroma, cervical or lumbar stenosis with compression myelopathy, polyneuropathy with severe proprioceptive impairment, Menier
  16. severe cardiovascular disease
  17. foot problems, lower limb amputation or joint arthrodesis
  18. terminal diseases (defined as estimated life expectancy of less than 6 months).

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Single Blind

30 participants in 1 patient group

balance treatment
Experimental group
Treatment:
Device: Self Mobility Improvement in the eLderly by using the SMILING system

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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