Dialectical Behaviour Group Therapy for Adults With Intellectual Disabilities
NCT ID: NCT02919826
Last Updated: 2020-06-02
Study Results
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View full resultsBasic Information
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COMPLETED
NA
20 participants
INTERVENTIONAL
2016-08-31
2018-03-31
Brief Summary
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Detailed Description
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This pilot intervention attempts to deliver and evaluate an adapted Dialectical Behavior Therapy (DBT) in group format. It is hypothesized that the strategies taught through this adapted modality will increase adults with dual diagnosis skills in managing difficult situations and their emotional reactions, thereby decreasing risk of crisis and ultimately demands placed on the mental health service system.
1.3 Research Questions:
Four key questions are addressed within this project:
1. Can adults with intellectual disabilities learn and retain knowledge and skills presented in an adapted DBT group program?
2. Do participants report positive increases in self-esteem and greater engagement in social situations following group participation?
3. Are there decreases in signs and symptoms of mental health issues i.e. anxiety and depression and improvements in challenging behavior following completion of the dialectical behavior group therapy program?
4. Does the program provide any benefit to caregivers? (e.g., are the able to de-escalate "crisis" situations quicker? Do caregivers feel it provides them tools to use when the client experiences distress? Does it lessen the caregivers stress?)
2\. Methods
2.1 Research Design:
Building upon the DBT adaptation work performed in the United States by Charleton and Dykstra (2011), it is necessary to further refine this intervention to increase its feasibility and viability as a treatment modality for the adult population with dual diagnosis. Using a mixed-methods approach within this current intervention allows exploration of DBT group therapy efficacy for adult with ID and emerging mental health/behavioural issues.
2.2 Recruitment:
Participants and caregivers will be invited to participate through the use of local advertising at partnering agencies and through expression of previous interest to clinicians involved. Information brochures/flyers will be distributed to individuals who have expressed an interest in counseling services and may or may not be receiving services at the time. Once participants have been identified they will have the opportunity to self-select a caregiver who they would like to assist them in the groups. The caregivers will receive a letter of information and consent form requesting their participation. All participants will be screened for eligibility and attainment of consent for involvement will include the use of a multi-modality approach.
Agencies to be recruited: Ongwanada, Providence Care MHS DDCOT, Christian Horizons, Community Living Kingston, Developmental Services Leeds and Grenville (DSLG), Pathways
2.3. Procedure
1. Recruit
2. Screen for Eligibility
3. Obtain Written Consent (to be confirmed at Pre-Assessment)
4. Complete Pre-Assessment and confirm informed Consent
a. At acceptance into the study, individuals will be assigned alpha-numeric symbols on all data documents to ensure patient confidentiality and ensure individuals are unidentifiable to research team. Individuals will be encouraged to use first names only during group sessions and all identifiers (name tags, sign in sheets) will be destroyed at the end of the treatment trial.
5. Once have n=12 participants, Randomize into Group A Intervention or Control
6. Send info package with date/location of group
7. Group A (Duration: 12 weeks)
a. Divided into 3 modules (Distress Tolerance; Emotion Regulation; Interpersonal Effectiveness, with Mindfulness integrated into each
8. Post Assessment of Group A Participants (n=6) and n=6 new participants
9. Repeat steps 4 to 8 for Group B and C 12-week intervention and control groups.
2.6 Analysis:
Global and individual change question analyses will be conducted within a mixed method approach using SPSS 22. Measures of pre-post group findings will be evaluated using paired t-tests and ANOVAS, if applicable. Structured interview data will be analyzed using thematic analysis where qualitative themes will be summarized and consolidated into possible areas addressing curriculum content, therapeutic process, skill application and overall group therapy feedback
Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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DBT Group
Adapted Dialectical Behaviour Therapy
Adapted Dialectical Behaviour Therapy
12 weekly sessions of DBT group therapy
Control Arm
People in this group will receive treatment as usual
No interventions assigned to this group
Interventions
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Adapted Dialectical Behaviour Therapy
12 weekly sessions of DBT group therapy
Eligibility Criteria
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Inclusion Criteria
* Symptoms of emotional and behavioural difficulties e.g. emotional dysregulation
* Dedicated caregiver to accompany and attend all sessions
Exclusion Criteria
* Profound or Severe Intellectual Disability
* Acute psychosis interfering with daily functioning
18 Years
75 Years
ALL
No
Sponsors
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Providence Health & Services
OTHER
Dr. Jessica Jones
OTHER
Responsible Party
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Dr. Jessica Jones
Principal Investigator
Principal Investigators
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Jessica Jones, PhD
Role: PRINCIPAL_INVESTIGATOR
Queen's University, Kingston
Locations
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Division of Developmental Disabilities, 191 Portsmouth Avenue
Kingston, Ontario, Canada
Countries
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Provided Documents
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Document Type: Study Protocol and Statistical Analysis Plan
Other Identifiers
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PSIY-511-15
Identifier Type: -
Identifier Source: org_study_id
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