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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02677766
Other study ID # TO_EFFI15_14
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 2016
Est. completion date October 20, 2017

Study information

Verified date September 2019
Source University of Modena and Reggio Emilia
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To date, there are no studies that demonstrate that the intervention of Occupational Therapy (OT) in patients considered to be complex, regardless of diagnosis, could improve clinical and functional outcome for the patient. For this reason, the investigators propose one randomized controlled trial that will compare the group receiving the intervention of OT and the control group, to quantify the level of performance and satisfaction in the activities of interest of the patient, identified through the COPM. The hypothesis is that the benefit may be higher, as clinically relevant, in the group of complex patients treated with the proposed intervention of OT compared to those receiving the usual rehabilitation therapy.


Description:

The investigators already implemented an observational pilot study, aimed at defining the characteristics and needs of the population in question and the OT intervention characteristics. These information will now be used to implement this randomized controlled trial, designed to demonstrate the effectiveness of the OT intervention on the basis of clinically relevant outcome measures.

This study will be set with exploratory purposes, with appropriate high number, which will allow the investigators to quantify the difference between the two groups in terms of performance scores derived from the COPM (COPM_p). From the results of this part it will then depend on the planning for the subsequent study with the correct sample size.


Recruitment information / eligibility

Status Completed
Enrollment 40
Est. completion date October 20, 2017
Est. primary completion date October 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years to 100 Years
Eligibility Inclusion Criteria:

- complex inpatient

Exclusion Criteria:

- primary psychiatric disorders,

- language barriers,

- severe cognitive impairment

- communication disability

Study Design


Related Conditions & MeSH terms

  • Complex Patients in Rehabilitation Phase

Intervention

Other:
occupational therapy
an intervention phase in the period of hospitalization for rehabilitation in the hospital, aimed mainly at achieving objectives related to the area of self-care and, secondly, the objectives in the areas of productivity and leisure, identified at T0; plus an intervention in the post-discharge at the patient's home, aimed primarily at achieving objectives related to the areas of productivity and leisure time and, secondly, to possible targets in residues of self-care, identified in T0.
Usual care
Usual care consists in rehabilitation treatment delivered by a multidisciplinary team

Locations

Country Name City State
Italy Arcispedale Santa Maria Nuova Reggio Emilia RE

Sponsors (2)

Lead Sponsor Collaborator
Stefania Costi Arcispedale Santa Maria Nuova-IRCCS

Country where clinical trial is conducted

Italy, 

References & Publications (1)

Pellegrini M, Formisano D, Bucciarelli V, Schiavi M, Fugazzaro S, Costi S. Occupational Therapy in Complex Patients: A Pilot Randomized Controlled Trial. Occup Ther Int. 2018 Sep 3;2018:3081094. doi: 10.1155/2018/3081094. eCollection 2018. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Change From Baseline to Follow-up of the Performance Score at the Canadian Occupational Performance Measure The Canadian Occupational Performance Measure is a valid, evidence-based outcome measure designed to capture a client's self-perception of performance in everyday living, over time.
The score is between 1 and 10, where 1 indicates poor performance and low satisfaction, respectively, while 10 indicates very good performance and high satisfaction
T0 is the baseline at the patient ammission in the rehabilitation Ward; T2 is the follow-up at end of the intervention, 45 days ± 15 days from discharge