An Exploratory RCT of a Psychosocial Group Intervention for Epilepsy (PIE)
Primary Purpose
Epilepsy
Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Psychosocial Intervention Group
Waiting list control
Sponsored by
About this trial
This is an interventional supportive care trial for Epilepsy focused on measuring Epilepsy, psychosocial
Eligibility Criteria
Inclusion Criteria:
- Written informed consent
- Diagnosis of epilepsy (controlled or refractory) of at least 6 months duration
- Between the ages of 1217 years old
- Have a reasonable level of expressive and receptive English language abilities to enable them to fully participate and contribute to the group process
- In mainstream schooling.
Exclusion Criteria:
- Formal diagnosis of Learning Disability or attendance at a school for children with Special Educational Needs
- Complex and severe mental health problems;
- Diagnosis of nonepileptic seizures in the absence of epileptic seizures
Epilepsies occurring in the context of:
- Postnatally acquired structural lesions (e.g. TBI or neurooncological conditions)
- Immune mediated disorders (e.g. limbic or antiNMDAR encephalopathy)
- Metabolic disorders (e.g. GLUT1 deficiency)
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Other
Arm Label
Psychosocial group intervention
Waiting List control
Arm Description
Participants in the waiting list control will continue in TAU but will then start the intervention once the first group of participants have completed the 3 month follow up in the psychosocial group intervention arm.
Outcomes
Primary Outcome Measures
Effectiveness of the PIE group
Comparing participant's quality of life at baseline, completion of intervention, and at 3 and 6 month post group completion, as measured via the GEOSYP and PedsQL
Effectiveness of the PIE group
Effectiveness of the PIE group
Effectiveness of the PIE group
Secondary Outcome Measures
The Paediatric Index of Emotional Distress (PIED).
The Seizure Self Efficacy Scale for Children (SSEC)
Epilepsy Knowledge ProfileGeneral (EKPG)
Brief Illness Representations Questionnaire (BIPQ).
Participant social functioning
seizure control
Full Information
NCT ID
NCT02349529
First Posted
January 19, 2015
Last Updated
January 23, 2015
Sponsor
NHS Greater Glasgow and Clyde
1. Study Identification
Unique Protocol Identification Number
NCT02349529
Brief Title
An Exploratory RCT of a Psychosocial Group Intervention for Epilepsy
Acronym
PIE
Official Title
An Exploratory Randomised Controlled Trial of a Manualised Psychosocial Group Intervention for Young People With Epilepsy (PIE)
Study Type
Interventional
2. Study Status
Record Verification Date
January 2015
Overall Recruitment Status
Unknown status
Study Start Date
February 2015 (undefined)
Primary Completion Date
April 2016 (Anticipated)
Study Completion Date
April 2016 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
NHS Greater Glasgow and Clyde
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Children and young people with epilepsy are at increased risk of poorer outcomes related to emotional and psychological adjustment, peer relationship problems, lower academic attainment and mental health problems across the lifespan. Despite the well understood risks, there continues to be a lack of psychological and psychosocial support for young people with epilepsy, and a corresponding lack of evidence regarding the effectiveness of psychosocial interventions. This study aims to evaluate a manualised psychosocial group intervention for adolescents with epilepsy. A cognitive behaviour therapy approach is used, aimed at increasing awareness of how epilepsy may impact upon thoughts, feelings and activities and to develop strategies for improved psychological adjustment. In addition, an epilepsy knowledge component aimed at improving a sense of control and epilepsy self-management is included. A group delivery format allows an opportunity for social modelling, and social problem solving, helping others and relating to other young people with similar experiences. The social learning context and availability of knowledgable facilitators (an epilepsy nurse specialist and clinical psychologist) are also key aspects of the intervention. The study will allow us to establish a standard manualised group intervention that can be used throughout the UK which aims to; establish the effectiveness and desirability of this approach; improve the overall quality of life, psychological health and social integration of young people with epilepsy; and to improve epilepsy knowledge and selfmanagement skills aimed at maximising seizure control and overall management.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Epilepsy
Keywords
Epilepsy, psychosocial
7. Study Design
Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
200 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Psychosocial group intervention
Arm Type
Experimental
Arm Title
Waiting List control
Arm Type
Other
Arm Description
Participants in the waiting list control will continue in TAU but will then start the intervention once the first group of participants have completed the 3 month follow up in the psychosocial group intervention arm.
Intervention Type
Behavioral
Intervention Name(s)
Psychosocial Intervention Group
Intervention Description
6 group sessions
Intervention Type
Other
Intervention Name(s)
Waiting list control
Intervention Description
Treatment as usual
Primary Outcome Measure Information:
Title
Effectiveness of the PIE group
Description
Comparing participant's quality of life at baseline, completion of intervention, and at 3 and 6 month post group completion, as measured via the GEOSYP and PedsQL
Time Frame
Baseline
Title
Effectiveness of the PIE group
Time Frame
6 weeks
Title
Effectiveness of the PIE group
Time Frame
3 months
Title
Effectiveness of the PIE group
Time Frame
6 months
Secondary Outcome Measure Information:
Title
The Paediatric Index of Emotional Distress (PIED).
Time Frame
Baseline, 6 weeks, 3 months and 6 months
Title
The Seizure Self Efficacy Scale for Children (SSEC)
Time Frame
Baseline, 6 weeks, 3 months and 6 months
Title
Epilepsy Knowledge ProfileGeneral (EKPG)
Time Frame
Baseline, 6 weeks, 3 months and 6 months
Title
Brief Illness Representations Questionnaire (BIPQ).
Time Frame
Baseline, 6 weeks, 3 months and 6 months
Title
Participant social functioning
Time Frame
Baseline, 6 weeks, 3 months and 6 months
Title
seizure control
Time Frame
Baseline, 6 weeks, 3 months and 6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
12 Years
Maximum Age & Unit of Time
17 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Written informed consent
Diagnosis of epilepsy (controlled or refractory) of at least 6 months duration
Between the ages of 1217 years old
Have a reasonable level of expressive and receptive English language abilities to enable them to fully participate and contribute to the group process
In mainstream schooling.
Exclusion Criteria:
Formal diagnosis of Learning Disability or attendance at a school for children with Special Educational Needs
Complex and severe mental health problems;
Diagnosis of nonepileptic seizures in the absence of epileptic seizures
Epilepsies occurring in the context of:
Postnatally acquired structural lesions (e.g. TBI or neurooncological conditions)
Immune mediated disorders (e.g. limbic or antiNMDAR encephalopathy)
Metabolic disorders (e.g. GLUT1 deficiency)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Liam Dorris, BSc (Hons), D.Clin.Psy
Phone
01412010638
Email
liam.dorris@ggc.scot.nhs.uk
First Name & Middle Initial & Last Name or Official Title & Degree
Helen Broome, BSc (Hons), D.Clin.Psy
Phone
01412010638
Email
helen.broome@ggc.scot.nhs.uk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Liam Dorris, BSc (Hons), D.Clin.Psy
Organizational Affiliation
NHS Greater Glasgow and Clyde
Official's Role
Principal Investigator
12. IPD Sharing Statement
Learn more about this trial
An Exploratory RCT of a Psychosocial Group Intervention for Epilepsy
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