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A Psychoeducational Intervention for Stroke Family Caregivers

The Chinese University of Hong Kong logo

The Chinese University of Hong Kong

Status

Completed

Conditions

Stroke

Treatments

Behavioral: Psychoeducation

Study type

Interventional

Funder types

Other

Identifiers

NCT02080910
CRE-2012.185-T

Details and patient eligibility

About

This is a randomized controlled trial with a 3-month psychoeducational program as intervention, followed by a 3 month observational period. The purpose of this study was to examine whether a psychoeducational program focusing on equipping caregivers with problem-solving skills would improve caregiver's problem-solving abilities, their psychological responses and caregiving resources, and would minimize the use of health and social services among stroke survivors.

Enrollment

128 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria (caregiver):

  • Family member of stroke survivor
  • Chinese adult
  • Live with stroke survivors
  • Primary caregiver
  • Being able to communicate with the researcher

Inclusion Criteria (stroke survivor):

  • Chinese adult with diagnosis of stroke
  • Live at home after discharge
  • Being able to understand and to give consent

Exclusion Criteria (caregiver and stroke survivor):

  • History of self-reported doctor-diagnosed psychiatric illness
  • (stroke survivor): being mild to totally independent

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

128 participants in 2 patient groups

Psychoeducational program
Experimental group
Description:
Psychoeducational program consisted of (1) two inpatient sessions of face-to-face education on stroke and its caregiving; (2) six biweekly problem-solving training via telephone contacts after the discharge of stroke survivors
Treatment:
Behavioral: Psychoeducation
Usual care
No Intervention group

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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