Meaning-based Group Counselling for Bereavement

Sponsor
Jewish General Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT01384942
Collaborator
McGill University (Other), Canadian Institutes of Health Research (CIHR) (Other)
26
1
2
40
0.6

Study Details

Study Description

Brief Summary

Given that individuals in bereavement tend to experience substantial psychological distress in the first two years following loss, individuals seeking psychological support will need appropriate services grounded in sound empirical scholarship. There is a lack of studies assessing bereavement groups, despite groups being one of the most common forms by which such services are offered. The prominent and emerging process of meaning-reconstruction in bereavement research is theorized to lead to better psychological adjustment and prevent more prolonged grief reactions. The principal objective of this study is to compare two types of group counseling for individuals in bereavement: A novel meaning-based bereavement counseling group and a conventional bereavement support group.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Meaning-Based Bereavement Group
  • Behavioral: Conventional Bereavement Group
Phase 2

Study Design

Study Type:
Interventional
Actual Enrollment :
26 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Supportive Care
Official Title:
The Development and Pilot Testing of Meaning-based Group Counselling Intervention for Bereavement
Study Start Date :
Jun 1, 2010
Actual Primary Completion Date :
Mar 1, 2012
Actual Study Completion Date :
Oct 1, 2013

Arms and Interventions

Arm Intervention/Treatment
Experimental: Meaning-Based Bereavement Group

Behavioral: Meaning-Based Bereavement Group
A 12 week bereavement counselling group with tasks and themes that focus on re-constructing meaning following death.

Active Comparator: Conventional Bereavement Group

Behavioral: Conventional Bereavement Group
An 8 week traditional bereavement group that follows a more conventional approach to grief support.

Outcome Measures

Primary Outcome Measures

  1. Grief [24 weeks]

    Descriptive statistical analysis (e.g., means, standard deviations, percentage of scale range improvements) will be conducted on the pre-test, post-test, and follow-up scores for both the experimental and control group on the following outcome measures (1) Grief: Revised Grief Experience Inventory; Core Bereavement; Hogan Grief Reaction Checklist

  2. Meaning [24 weeks]

    Descriptive statistical analysis (e.g., means, standard deviations, percentage of scale range improvements) will be conducted on the pre-test, post-test, and follow-up scores for both the experimental and control group on the following outcome measures (1) Meaning: Purpose in Life Test; The Grief and Meaning-Reconstruction Inventory; The Integration of Stressful Life Experiences Scale

  3. Depression [24 Weeks]

    Descriptive statistical analysis (e.g., means, standard deviations, percentage of scale range improvements) will be conducted on the pre-test, post-test, and follow-up scores for both the experimental and control group on the following outcome measures (1) Depression: Center for Epidemiologic Studies Depression Scale

  4. Anxiety [24 Weeks]

    Descriptive statistical analysis (e.g., means, standard deviations, percentage of scale range improvements) will be conducted on the pre-test, post-test, and follow-up scores for both the experimental and control group on the following outcome measures (1)Anxiety: State-Trait Anxiety Scale

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Individuals presenting for bereavement services that have experienced a death-related loss within 6 weeks to 2 years of the first meeting of the group, and are experiencing an uncomplicated grief response will be invited to participate.

  • Individuals will be assessed for their ability to participate in a group counselling context as well as an uncomplicated grief trajectory. Participants must be 18 years of age or older, have sufficient ability to communicate in English, as well as read English.

Exclusion Criteria:
  • Following a clinical/diagnostic interview and administration of the PG-13 (Prolonged Grief Disorder-13, Prigerson et al., 2009), individuals experiencing a complicated/prolonged grief trajectory are excluded.

  • Furthermore, individuals whose cognitive condition might make the study burdensome or impossible for them are excluded.

Contacts and Locations

Locations

Site City State Country Postal Code
1 S.M.B.D. Jewish General Hospital / Hope and Cope Program Montreal Quebec Canada H3T 1E2

Sponsors and Collaborators

  • Jewish General Hospital
  • McGill University
  • Canadian Institutes of Health Research (CIHR)

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Christopher J. MacKinnon, Psychologist, Jewish General Hospital
ClinicalTrials.gov Identifier:
NCT01384942
Other Study ID Numbers:
  • 002645
  • NCT01285128
First Posted:
Jun 29, 2011
Last Update Posted:
Nov 8, 2013
Last Verified:
Aug 1, 2013
Keywords provided by Christopher J. MacKinnon, Psychologist, Jewish General Hospital

Study Results

No Results Posted as of Nov 8, 2013