Skip to main content
Clinical Trials/NCT03409354
NCT03409354CompletedNot Applicable

Tele-Rehabilitation Pilot Evaluation Study

National University of Singapore2 sites in 1 country14 target enrollmentStarted: May 15, 2018Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
14
Locations
2
Primary Endpoint
Adherence to rehabilitation over the course of a 2 week trial period

Study Overview

Brief Summary

A proof of concept randomized controlled trial (RCT) only evaluated the National University of Singapore's (NUS) T-Rehab tele-rehabilitation (TR) system at a home setting where rehabilitation was provided on an individual level. The previous RCT was also limited to stroke patients. In addition to stroke, there are many other conditions (such as fractures, lower limb joint replacement, musculoskeletal conditions) require and benefit from rehabilitation. The primary aims of the pilot evaluation study are: (i) To document patient adherence to TR, compared to usual care (ii) To estimate the extent to which TR improves functional status, compared to usual care and (iii) To estimate the cost effectiveness of TR, compared to usual care in eight different health conditions in Singapore.

Detailed Description

This is a 12-week quasi-experimental trial of a tele-rehabilitation program involving seven sites and up to 600 adults in Singapore.

Study Design

Study Type
Interventional
Allocation
Non Randomized
Intervention Model
Parallel
Primary Purpose
Health Services Research
Masking
None

Eligibility Criteria

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

Inclusion Criteria

  • at least 21 years of age
  • Admitted into an inpatient or outpatient rehabilitation unit, nursing home or day care centre for an acute or chronic disability
  • Deemed by any members of the multi-disciplinary rehabilitation team to potentially able to safely receive and benefit from rehabilitation post-discharge
  • Cognitively able to understand and follow instructions (the Abbreviated Mental Test's score of 6 or above (out of 10).

Exclusion Criteria

  • Patients with previous seizure episodes
  • Patients with limb musculoskeletal pain of at least moderate intensity (visual analogue Scale > 6 out of 10)
  • Patients with pacemakers.

Arms & Interventions

Tele-rehabilitation

Experimental

Tele-rehabilitation via iPad.

Intervention: Tele-rehabilitation (Behavioral)

Usual care

Active Comparator

Usual rehabilitation care, prescribed by rehabilitation therapists at participating centers and performed by participants at participating centers.

Intervention: Usual care (Behavioral)

Outcomes

Primary Outcomes

Adherence to rehabilitation over the course of a 2 week trial period

Time Frame: At 12-weeks post-rehabilitation

Adherence to the prescribed rehabilitation and exercise therapy will be measured over 12 weeks

Secondary Outcomes

  • EQ-5D(12-weeks)
  • IADL(12-weeks)
  • Health Service Utilization(12-weeks)
  • CESD(12-weeks)
  • Barthel Index(12-weeks)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Miho Asano

Assistant Professor

National University of Singapore

Study Sites (2)

Loading locations...

Similar Trials