A Trial of a Client-centered Intervention Aiming to Improve Functioning in Daily Life After Stroke

NCT01417585 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 280

Last updated 2013-04-16

No results posted yet for this study

Summary

This is a cluster randomized controlled trial in which client-centered rehabilitation of activities of daily living (CADL) will be compared to usual rehabilitation of activities of daily living (UADL) regarding participation in activities of daily living, independence in activities of daily living and life satisfaction during the first year after stroke. In addition use of health services, caregiver burden and significant others' life satisfaction will be studied. Study design, methods and power analysis are based on our previous pilot study. Participating rehabilitation centers in the counties of Stockholm, Uppsala and Gavleborg have been randomized to supply CADL or UADL. Patients are included who are: \< 3 months after stroke, dependent in at least two activities of daily living, understand instructions and referred to a participating rehabilitation unit. Data are collected at baseline, 3, 6 and 12 months. For sufficient power 280 participants will be included. In addition qualitative longitudinal studies will be performed in order to describe how CADL is integrated.

Conditions

  • Stroke
  • Physical Disability
  • Multiple Disability

Interventions

BEHAVIORAL

Client-centered ADL intervention

Client-centered ADL refers to rehabilitation of activities of daily living specifically guided by the needs as expressed by the client/patient and her/his significant others, a process that specifically aims to support the client by taking the client's goals and views as the guide for the rehabilitation process.

BEHAVIORAL

Usual ADL intervention

The variation of strategies and ways to conduct usual ADL rehabilitation according to the routines and praxis of the participating rehabilitation units randomized to supply the control condition.

Sponsors & Collaborators

  • The Swedish Research Council

    collaborator OTHER_GOV
  • Swedish Council for Working Life and Social Research

    collaborator OTHER
  • The Swedish Brain Foundation (Hjärnfonden)

    collaborator UNKNOWN
  • Stroke-Riksförbundet

    collaborator UNKNOWN
  • Region Stockholm

    collaborator OTHER_GOV
  • Uppsala County Council, Sweden

    collaborator OTHER_GOV
  • Uppsala-Örebro Regional Research Council

    collaborator OTHER
  • Karolinska Institutet

    lead OTHER

Principal Investigators

  • Kerstin Tham, PhD · Karolinska Institutet

Study Design

Allocation
RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
SINGLE
Model
PARALLEL

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-09-30
Primary Completion
2012-09-30
Completion
2012-12-31

Countries

  • Sweden

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01417585 on ClinicalTrials.gov