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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
NHS Greater Glasgow and Clyde
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Epilepsy focused on measuring Epilepsy, psychosocial

Eligibility Criteria

12 Years - 17 Years (Child)All SexesDoes not accept healthy volunteers

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:

    1. Postnatally acquired structural lesions (e.g. TBI or neurooncological conditions)
    2. Immune mediated disorders (e.g. limbic or antiNMDAR encephalopathy)
    3. 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

    First Posted
    January 19, 2015
    Last Updated
    January 23, 2015
    Sponsor
    NHS Greater Glasgow and Clyde
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    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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