Outcome Study of Hold Me Tight Program With Acquired Brian Injury (ABI) Populations

March 6, 2012 updated by: Nova Scotia Health Authority

Pilot Study of the Hold Me Tight Relationship Enhancement Program With Couples Where One Partner Has an Acquired Brian Injury

The objectives of this research pilot project are to assess the efficacy of the Hold Me Tight Relationship Enhancement Program with couples where at least one partner has an acquired brain injury.

Study Overview

Status

Withdrawn

Intervention / Treatment

Detailed Description

Families, and spouses in particular, have been shown to play important roles in all aspects of health care, especially when family members are recovering from the trauma of sudden illness or an accident such as a brain injury. A limited body of evidence suggests couple therapy provides patients and their spouses with the opportunity to explore the experience of trauma as it relates to becoming physically disabled within the context of intimate relationships. Being in close contact and emotionally connected to a person who has experienced trauma becomes a chronic stressor that can cause family members to experience trauma symptoms themselves. This phenomenon is termed secondary traumatic stress. For example, children can mimic a parent's trauma responses through identification with the parent or direct training. This is a specific type of secondary traumatisation transmitted intergenerationally.

The research about individuals who have a traumatic brain injury (TBI) and the impact of the injury on family functioning has outlined a number of challenges including: psychological distress, particularly anxiety and depression, among caregivers; disruptions in family functioning; and the impact on relationships including caregiver burden. Furthermore, among the most difficult conditions for couples to deal with are those involving cognitive impairment.

Hold Me Tight is a couples enrichment program that is based on the Emotionally Focused Therapy (EFT) approach to working with couples. EFT is an empirically supported treatment that arose out of emotion theory and attachment theory. It views emotions as centrally important in the experience of self, in both adaptive and maladaptive functioning, and in therapeutic change. From the EFT perspective change occurs by means of awareness, regulation, reflection, and transformation of emotion taking place within the context of an empathetically attuned relationship. There is significant research on this approach and it has been found that 70-75% of couples move from distress to recovery and that the gains are sustained for months to years following the end of treatment. As such, EFT is an evidence based treatment protocol.

Study Type

Interventional

Phase

  • Phase 3

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Nova Scotia
      • Halifax, Nova Scotia, Canada, B3H 4K4
        • Nova Scotia Rehabilitation Centre

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Participants must:
  • be over the age of 18;
  • be in a relationship at least 24 months and must be living together
  • be at least 12 months post brain injury event
  • be able to read and understand English, follow verbal instructions and provide verbal answers to questions;
  • be able to follow-up as per Hold Me Tight program protocol;
  • be willing to take part in the study, including completing all questionnaires before and after the intervention;
  • are competent to give informed consent as determined by the Investigators

Exclusion Criteria:

  • Participants must NOT:
  • suffer from severe aphasia or dementia as determined by health chart;
  • have active psychiatric illness;
  • have other neurological condition(s);
  • be couples where both partners have sustained a brain injury;
  • have a high level of relationship distress better served by seeking individual couple therapy as indicated by a DAS score of 70 or less for either member of a couple

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Supportive Care
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Relationship enhancement group
One group, all involved in the intervention
Relationship enhancement group

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Dyadic Adjustment Scale (DAS)
Time Frame: Change from Baseline in DAS scores at the end of the intervention and at three month follow-up
Change from Baseline in DAS scores at the end of the intervention and at three month follow-up
Beck Depression Inventory (BDI)
Time Frame: Change from Baseline in BDI scores at the end of the intervention and at three month follow-up
Change from Baseline in BDI scores at the end of the intervention and at three month follow-up
Beck Anxiety Inventory (BAI)
Time Frame: Change from Baseline in BAI scores at the end of the intervention and at three month follow-up
Change from Baseline in BAI scores at the end of the intervention and at three month follow-up

Secondary Outcome Measures

Outcome Measure
Time Frame
Hold Me Tight Conversations Rating Scale
Time Frame: 12 weeks and three month follow-up
12 weeks and three month follow-up
Hold Me Tight Program Evaluation
Time Frame: 12 weeks
12 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Collaborators

Investigators

  • Principal Investigator: Robert J Allan, M.Ed., Dalhousie University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

January 1, 2012

Primary Completion (Anticipated)

April 1, 2012

Study Completion (Anticipated)

July 1, 2012

Study Registration Dates

First Submitted

July 27, 2011

First Submitted That Met QC Criteria

July 27, 2011

First Posted (Estimate)

July 29, 2011

Study Record Updates

Last Update Posted (Estimate)

March 7, 2012

Last Update Submitted That Met QC Criteria

March 6, 2012

Last Verified

September 1, 2011

More Information

Terms related to this study

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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