The effect of family-centered empowerment model on persons with SCI on quality of life and health behaviors

Not Applicable

Recruiting

• Conditions: Individual with Spinal Cord Injury (Paraplegia).; Other and unspecified injuries of thoracic spinal cord, Other and unspecified injury of lumbar and sacral spinal cord; S24.1, S34

• Registration Number: IRCT20120804010488N3
• Lead Sponsor: Brain and spinal cord injury reseach center

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 21 May 2018

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 48

Inclusion Criteria

Inclusion criteria for Individual with Spinal Cord Injury (SCI): Participants who had spinal cord injury from type of paraplegia by the diagnosis of a specialist physician
those who had age of more than 18 years
those who had spinal cord injury more than one year and less than 5 years
those who had mental and cognitive ability
those who had the ability to read and write
Inclusion criteria for family caregivers: Participants who were family caregiver that being aware of the Individual with SCI’s condition
those who were not a member of the medical team
those who had mental and cognitive ability
those who had ability for reading and writing

Exclusion Criteria

Participants who had fractures in the bones and amputations; Participants who had pregnancy and / or surgery and coma from the past year

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Quality of life for spinal cord injury person. Timepoint: At the beginning of the study; one month later; three months later. Method of measurement: Quality of life questionnaire for the person with spinal cord injury (Frans and Powers) and general quality of life questionnaire (Frans and Powers).;Health behaviors. Timepoint: At the beginning of the study; one month later; three months later. Method of measurement: Health behavior questionnaire.;Quality of life for family caregivers. Timepoint: At the beginning of the study; one month later; three months later. Method of measurement: General quality of life questionnaire (Frans and Powers).