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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01957358
Other study ID # GR2013
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date October 2013
Est. completion date June 2020

Study information

Verified date April 2019
Source University of Manitoba
Contact Gail Burnside
Phone (204) 786-4753
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to examine the usefulness of the Grief Recovery Method in assisting persons with spinal cord injuries to achieve as complete a recovery as possible, thereby allowing for fuller participation in life.


Recruitment information / eligibility

Status Recruiting
Enrollment 8
Est. completion date June 2020
Est. primary completion date December 2019
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

* Persons with a spinal cord injury who are willing to participate in the program.

Exclusion Criteria:

* Unable or unwilling to participate.

Study Design


Intervention

Behavioral:
The Grief Recovery Method
The Grief Recovery Method is a structured process designed to help people with spinal cord injuries examine their knowledge of their injury, their emotional reaction to their injury, and their ability to acknowledge their grief over the injury in order to learn techniques to resolve the grief in order to achieve a more complete recovery. Participants will attend a total of 18 sessions, some one-on-one, and some in a group setting. The Grief Recovery Handbook, handouts, DVD (digital video disc) presentations and questionnaires will be used. Targeted activities to decrease isolation and assist volunteers to identify goals for recovery will be utilized.

Locations

Country Name City State
Canada WRHA Health Sciences Centre Rehabilitation Hospital Winnipeg Manitoba

Sponsors (1)

Lead Sponsor Collaborator
Dr. Karen Ethans

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Impact of Event Scale A self-administered questionnaire with 22 questions designed to measure the subjective response to a specific traumatic event (for this study, the event is the spinal cord injury). At Sessions 1 and 18. (Baseline and month 4)
Secondary Modified Grief Inventory A self-reported 2-part questionnaire that asks the volunteer to circle responses to questions about past behavior and present feelings about their spinal cord injury. At Sessions 1and 18 (baseline and month 4).
Secondary The Coping with Health Injuries and Problems A 32-question self-reported scale that measures coping with illness. At sessions 1 and 18 (Baseline and month 4)
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