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Clinical Trial Summary

Since the post-acute phase, patients have occupational needs related to social reintegration, that improve the autonomy, social roles in family, at work and in the community. Unmet needs could lead to a lower level of social reintegration. Healthcare professionals should be able to recognize the level of social reintegration of complex patients discharged from the Physical Medicine Rehabilitation (PRM) unit with the aim to identify those who need intervention aimed at improving social reintegration. The preliminary Italian version of the RNL index (RNLI) will describe the social reintegration level of the target population, once its psychometric properties will be tested.


Clinical Trial Description

The investigators will recruit three groups of participants to test the psychometric properties of the Italian version of the RNLI: complex patients, caregivers and stakeholders. Phase_1: to test the Content validity. The content validity will be tested on 10 complex patients and 10 stakeholders, who will assess the clarity and relevance of the RNLI items, respectively. In this phase, complex patients are hospitalized in the PMR unit. From this first phase, the investigators will obtain the preliminary Italian version of the RNLI to test its psychometric properties. Phase_2: to test the Reliability, Construct validity and Responsiveness. During the hospitalization in the PMR unit, 138 patients and their caregivers will be recruited. During this phase, the investigators will detect the important occupational activities of complex patients enrolled through a semi-structured interview conducted in person. After discharge, the investigators will contact the patients and their caregivers by telephone at different times (T0, T1 and T2) to test the following psychometric properties through the administration of the Italian version of the RNLI and the Canadian Occupational Performance Measure (COPM). Caregiver will have to answer to the RNLI as a proxy for the patient. The contact times and the psychometric properties that will be tested are: T0_ 2 weeks after discharge - internal consistency - inter-observer reliability - convergent construct validity T1_ 10-14 days after T0 - test-retest reliability T2_ 6-8 weeks after T0 - discriminant construct validity - responsiveness ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04450225
Study type Observational
Source Azienda Unità Sanitaria Locale Reggio Emilia
Contact Martina Pellegrini
Phone +39 0522295189
Email martina.pellegrini@ausl.re.it
Status Recruiting
Phase
Start date July 13, 2020
Completion date November 2023

See also
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