Group Based Treatment for Persons With Social Communication Difficulties

August 13, 2021 updated by: Silje Merethe Hansen, Sunnaas Rehabilitation Hospital

Group Based Treatment for Persons With Social Communication Difficulties: A Randomized Controlled Trial

A large proportion of patients with ABI have cognitive deficits that affect the way they communicate. Cognitive difficulties with attention, memory, executive functions and so on affect social communication. Without successful social skills, a person may engage in conflicts, become isolated and be denied access to social and vocational opportunities. Internationally, several group interventions have been developed for treating social communication difficulties during the last years.

Group Interactive Structured Treatment (GIST) is a validated holistic multidisciplinary group treatment targeting social communication skills after traumatic brain injury. The main aim of the present study is to examine the efficacy of GIST for improving social communication in persons with acquired brain injury, including TBI, stroke, tumor ect. Secondary the study aims to compare the standard GIST protocol to an newly developed intensive GIST protocol. Efficacy will be assessed immediately after intervention, but also three and six months after the intervention. The project is in line with international research efforts aimed to establish more knowledge about group treatment for persons with social communication disorders after ABI.

Study Overview

Status

Completed

Conditions

Study Type

Interventional

Enrollment (Actual)

49

Phase

  • Not Applicable

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

      • Nesoddtangen, Norway, 1450
        • Sunnaas rehabilitation hospital

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 to 75 years (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • traumatic brain injury (TBI), cerebrovascular accidents (stroke; CVA) patients with no concomitant diseases minimum 6 months post-injury
  • The patient are experiencing social communication disorders
  • The family member is experiencing the patients social communication disorders
  • The patient is motivated and expresses a desire to change communication behavior
  • One close family member is able to participate in the intervention process
  • Adequate Norwegian language proficiency to participate in the group
  • The patient experiences moderate to severe difficulties with minimum 3 aspects of communication assessed with La Trobe Questionnaire
  • The patient have insight into their communication difficulties (minimum intellectual insight) assessed with Awareness Questionnaire

Exclusion Criteria:

  • Age <18 years
  • Aphasia. Based on previous records.
  • Major psychiatric disorder or reported ongoing alcohol or substance abuse
  • Premorbid neurological disease or insult and/or comorbid neurological disease
  • Impaired basic linguistic, mnemonic, motor, or perceptual function that can interfere with the ability to engage with the training or intelligence quotient (IQ) < 85

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: TREATMENT
  • Allocation: RANDOMIZED
  • Interventional Model: PARALLEL
  • Masking: NONE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
EXPERIMENTAL: Standard GIST
Standard Group Interactive Structured Treatment.
13 group modules will be administered to outpatients in 12 x 2,5-3 hours sessions. Manualized intervention; In every group session a new topic is presented, discussed and practiced in group exercises. Homework assignments between sessions.
Other Names:
  • GIST
OTHER: Waitlist control/Intensive GIST
After a wait list control period of nine months the participants receive Intensive Group Interactive Structured Treatment.
13 group modules will be administered to inpatients during 4 weeks in hospital. Participants is admitted to a hospital unit for cognitive rehabilitation treating patients in acute and/or cronic phase. The participants are given extended leave every weekend to work on homework Assignments between each treatment week.
Other Names:
  • GIST

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
La Trobe Questionnaire.
Time Frame: Change from baseline up to 6 months
The LaTrobe Communication Questionnaire (LCQ) is a 30-item questionnaire that measures communication ability, a subjective outcome measure. Various communication behaviours are rated on a 4-point scale: 1¼never or rarely, 2¼sometimes, 3¼often and 4¼usually or always, but six items require a reverse in the scoring. Higher scores reflect reduced communications skills. The tool was developed to obtain information from various sources (e.g. self -rating by individual with TBI, rating by support person).
Change from baseline up to 6 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Profile of Pragmatic Impairment in Communication (PPIC)
Time Frame: Change from baseline up to 6 months
PPIC is an objective measure of social communication skills designed specifically for use with people with TBI. It includes 10 feature summary scales that assess communication skills on a 6-point scale from normative (0) to very severely impaired (5), with lower scores indicating better performance. These summary scales-logical content; general participation; quantity; quality; internal relation; external relation; clarity of expression; social style; subject matter; and aesthetics.
Change from baseline up to 6 months
Mind in the eyes test
Time Frame: Change from baseline up to 6 months
This test consists of 36 black- and-white pictures of the eye region. The images are presented one by one, along with four adjectives (one target word and three foil words).
Change from baseline up to 6 months
Goal Attainment Scaling (GAS)
Time Frame: Change from baseline up to 6 months

Goal Attainment Scaling (GAS) is a flexible system of measuring outcome goals, based on a 5-point scale.

Levels of goal attainment are expressed objectively in terms of concrete behaviors that can be observed and recorded.

Change from baseline up to 6 months
Behavior Rating Inventory for Executive Functions (BRIEF)
Time Frame: Change from baseline up to 6 months
BRIEF is a 75-item self and other questionnaire that measures executive functions (inhibition, shift, emotional control, self-monitoring, initiative, working memory, planning/organizing, task monitoring, organizing of materials)communication ability. Various executive behaviours are rated on a 3-point scale.
Change from baseline up to 6 months
Social competence checklist
Time Frame: Change from baseline up to 6 months
Is an interview where the participant and close family member answer 6 yes or no answers regarding the participants social communication skills. The interview is found in the GIST protocol developed by Hawley and Newman 2002.
Change from baseline up to 6 months
CIQ (Community Integration Questionnaire)
Time Frame: Change from baseline up to 6 months
The Community Integration Questionnaire (CIQ) is a community integration outcome measure developed for TBI subjects; its social integration and productivity subscales were used for this study. Frequency of such activities as shopping, leisure pursuits, visiting friends or relatives, travel, and one's work, school, or volunteer situation, are scored on a 15-item scale; a higher score indicates greater integration.
Change from baseline up to 6 months
Norwegian Version of the General Perceived Self-Efficacy Scale
Time Frame: Change from baseline up to 6 months
is a 20-item questionnaire that measures self-efficacy rated by a 4-point scale.
Change from baseline up to 6 months
Norwegian Quality of Life Scale (PQoL),
Time Frame: Change from baseline up to 6 months
is a 20-item questionnaire that measures quality of life, a subjective outcome measure. The quality of life is rated in a 0-10 point scale. Higher scores reflect high quality of life.
Change from baseline up to 6 months
Symptom Checklist (SCL-10)
Time Frame: Change from baseline up to 6 months
To document self-reported psychological problems and symptoms of psychopathology, the Symptom Checklist 90-R was used.
Change from baseline up to 6 months
Social Communication Questionnaire with additional questions (SCQ-A)
Time Frame: Change from baseline up to 6 months
SCQ-A is a 37-item questionnaire that measures communication ability, a subjective outcome measure. Various communication behaviours are rated on a 5-point scale. Higher scores reflect reduced communications
Change from baseline up to 6 months

Collaborators and Investigators

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

Collaborators

Investigators

  • Principal Investigator: Melanie Kirmess, PHD, Sunnaas Sykehus

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

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 (ACTUAL)

September 1, 2018

Primary Completion (ACTUAL)

June 16, 2020

Study Completion (ACTUAL)

June 16, 2020

Study Registration Dates

First Submitted

August 12, 2018

First Submitted That Met QC Criteria

August 15, 2018

First Posted (ACTUAL)

August 17, 2018

Study Record Updates

Last Update Posted (ACTUAL)

August 19, 2021

Last Update Submitted That Met QC Criteria

August 13, 2021

Last Verified

August 1, 2021

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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