Skip to main content
Clinical Trials/NCT03668938
NCT03668938
Completed
Not Applicable

Efficacy of Occupational Therapy in the Rehabilitation of Complex Patients: Randomized Controlled Trial

Azienda USL Reggio Emilia - IRCCS1 site in 1 country92 target enrollmentOctober 8, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Rehabilitation
Sponsor
Azienda USL Reggio Emilia - IRCCS
Enrollment
92
Locations
1
Primary Endpoint
Change in Reintegration to Normal Living Index
Status
Completed
Last Updated
10 months ago

Overview

Brief Summary

A previous study that involved the intervention of the occupational therapist (OT) on complex patients both in hospital and at home showed the effectiveness of OT during hospitalization. The effectiveness was not demonstrated in the post-discharge phase. Now, the investigators presented a RCT to compare the levels of social reintegration between the intervention group and control group. The hypothesis is that the intervention group obtains a higher and clinically relevant level of social reintegration compared to the group treated with the usual care.

Detailed Description

In the previous study, the intervention group achieved higher gains in the return to normal life than in the control group, but this difference did not reach statistical significance. Because of this, a new study was implemented with the correct sample size, defined through the previous study. In addition, the post-discharge phase the COPM was administered to define new objectives relating mainly to productivity and leisure time areas. Finally, the investigators have indentified some territorial services with the aim to create tailored paths/interventions for patients to promote social reintegration.

Registry
clinicaltrials.gov
Start Date
October 8, 2018
End Date
September 23, 2020
Last Updated
10 months ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Azienda USL Reggio Emilia - IRCCS
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Complex impatient
  • Admitted to AUSL-IRCCS/UO MFR

Exclusion Criteria

  • Language barriers
  • Severe cognitive impairment
  • Psychiatric disorders
  • Domiciled in a protected facility at the time of admission

Outcomes

Primary Outcomes

Change in Reintegration to Normal Living Index

Time Frame: Time 1 is on average 45 days from Time 0 (discharge from the rehabilitation ward); Time 2 is at 90 days ± 15 days from discharge

Compare the change in the level of reintegration to normal life between the two arms. The score range is from 1 to 100. Higher values represent a better outcome.

Secondary Outcomes

  • Canadian Occupational Performance Measure(Time 0 is the baseline at the patient ammission in the rehabilitation ward; Time 1 is on average 45 days from Time 0 (discharge from the rehabilitation ward); Time 2 is at 90 days ± 15 days from discharge)
  • Modified Barthel Index(Time 0 is the baseline at the patient ammission in the rehabilitation ward; Time 1 is on average 45 days from Time 0 (discharge from the rehabilitation ward); Time 2 is at 90 days ± 15 days from discharge)
  • Instrumental Activity of Daily Living(Time 0 is the baseline at the patient ammission in the rehabilitation ward; Time 1 is on average 45 days from Time 0 (discharge from the rehabilitation ward); Time 2 is at 90 days ± 15 days from discharge)
  • Hospital Anxiety and Depression Scale(Time 0 is the baseline at the patient ammission in the rehabilitation ward; Time 1 is on average 45 days from Time 0 (discharge from the rehabilitation ward); Time 2 is at 90 days ± 15 days from discharge)
  • Short Form 12(Time 1 is on average 45 days from Time 0 (discharge from the rehabilitation ward); Time 2 is at 90 days ± 15 days from discharge)

Study Sites (1)

Loading locations...

Similar Trials