Skip to main content
Clinical Trials/NCT06029361
NCT06029361RecruitingNot Applicable

Improving Function and Mobility in Geriatric Patients After a Femoral Neck Fracture Who Are Undergoing Inpatient Rehabilitation Using an Augmented Reality Practice System - SELFIT

Meir Medical Center2 sites in 1 country50 target enrollmentStarted: August 8, 2023Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Enrollment
50
Locations
2
Primary Endpoint
5 time sit to stand

Study Overview

Brief Summary

Type of study: prospective interventional the purposes of the research :To examine the effect of treatment using the SELFIT system on function, walking and balance in patients after hip fractures hospitalized in the geriatric rehabilitation department.

The study population: 50 participants aged 65+ who were admitted to the geriatric rehabilitation department after hip fractures, with 25 in the experimental group and 25 in the control group.

The main question[s] it aims to answer are:

  • What is the effect of training with SELFIT system on the functional outcomes in patients after hip fractures hospitalized in the geriatric rehabilitation department.
  • How the training with SELFIT system will effect on satisfaction of the patients in the geriatric rehabilitation department.

During 21 days, both groups will receive physical therapy for about 45 minutes. The experimental group will be allocated about 15 minutes out of the 45 minutes to practice with the help of the SELFIT system.

Detailed Description

Recruiting participants for the study:

When admitting patients hospitalized in the geriatric rehabilitation department after hip neck fractures, their suitability for participation in the study will be examined according to inclusion and exclusion criteria. Patients who meet the inclusion criteria will receive an explanation of the research procedure and its goals, and if they agree and are suitable in terms of signature competence and cognitive ability to participate in the study, they will sign an informed consent form for participation in the study.

After signing a consent form to participate in the study, each participant will be randomly assigned to an experimental group or a control group. After the patient agrees to participate in the study, he will receive a number that will be assigned in sequential order, where an even number means belonging to the experimental group and an odd number, belonging to the control group.

Intervention:

During 21 days, both groups will receive physical therapy for about 45 minutes. The experimental group will be allocated about 15 minutes out of the 45 minutes to practice with the help of the SELFIT system.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Masking Description

an assessment will be made by questionnaires and an objective assessment by physiotherapists who will not be involved in the treatment of the SELFIT system in the interventional group

Eligibility Criteria

Ages
65 Years to — (Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Ability to walk independently or under supervision before the fracture
  • Patients with full weight bearing on the operated leg according to the instructions of an orthopedic surgeon (FWB - Full Weight Bearing)
  • Patients who are able to walk with an assistive device FIM 3 and above (FIM Functional independence measure)
  • Mental competence after a comprehensive assessment by a Geriatric Specialist

Exclusion Criteria

  • Patients with cognitive decline following dementia or delirium
  • Patients with complications after surgery - infection or bleeding in the surgical area
  • Patients with previous neurological injury or current CNS disease.
  • Patients with a previous lower limb fracture in the last 5 years.

Outcomes

Primary Outcomes

5 time sit to stand

Time Frame: 9 month

Assessment of time performance for five time stand up and sitting on chair. Less time means better outcome

Berg Balance Test

Time Frame: 9 month

Assessment of balance function by 14 tasks. Min.0 max.56 points Higher score means better outcome.

Functional Independence Measure

Time Frame: 9 month

Measured by: Functional Independence Measure Index (FIM) that assess activity of daily living. only motor assessment part is used. Minimum score 5 pts. Maximum score: 35 points. Higher score means better outcome

10 Meter walk test

Time Frame: 9 month

Assessment of time performance of walking 10 meters. Less time means better outcome

Falls Efficacy Scale

Time Frame: 9 month

Assessment of confidence of functions. Score range from 16 to 64 points. Higher score means better outcomes

PTPSQ-H physical therapy satisfaction questionnaire

Time Frame: 9 month

Hebrew approved version. 15 questions about patient satisfaction with physical therapy care. Score range about 15 to 75. Higher score means better outcomes

VAS - visual analog scale

Time Frame: 9 month

as mesured by a pain scale from 1 to 10. Lower score means better outcome

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Alexander Protsenko

Head of physiotherapy of geriatric rehabilitation unit

Meir Medical Center

Study Sites (2)

Loading locations...

Similar Trials