- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02622048
Understanding and Helping Families: Parents With Psychosis
STAGE 1: Investigating Attributions and Expressed Emotion in Parents With and Without Psychosis STAGE 2: Investigating the Use of a Self-directed Parenting Programme With Parents Experiencing Psychosis
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The trial will be split into two stages.
Stage 1: Parents with no history of serious mental health problems and parents who have a history of psychosis or schizophrenia, who have children aged 3-10 years old, will take part in the Revised Five Minute Speech Sample (FMSS) and the Modified Camberwell Family Interview (CFI). They will also complete various measures looking at parental well-being, depression, anxiety and stress as well as parenting behaviours and interpretations of their child behaviour. In addition the PANSS interview will also be used. These interviews will be coded to investigate attributional patterns.
Stage 2: Parents who are experiencing psychosis, who took part in stage 1 will proceed to stage 2 if they want to. Parents will be seen weekly and take part in a guided self-help parenting intervention. This will require weekly visits over 10 weeks to the parents. During this time, symptoms, mood, general well-being and parenting behaviours will be monitored.
There will be no randomisation: all parents experiencing psychosis will receive the intervention.
Children do not attend the sessions, but it is hoped that parents practice the skills learned.
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Lancashire
-
Manchester, Lancashire, United Kingdom, M139PL
- Recruiting
- The University of Manchester
-
Contact:
- Lauren Stockton
- Phone Number: 01613062619
-
Principal Investigator:
- Lauren Stockton
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria for parents with psychotic illnesses
- Presence of ICD-10 schizophrenia-spectrum diagnosis (F20-29).
- Primary parental caregiver for index child. This includes 10 hours of contact time with their child.
- Over 18 years of age.
- Have at least one child aged 3-10 years old.
- Identify difficulties in parenting during assessment.
- Proficient in written and spoken English.
- Capacity to provide informed consent.
Exclusion Criteria for parents with psychotic illnesses
- Parents with a schizophrenia-spectrum diagnosis who have recently been discharged from acute in-patient care, and have less than four weeks of stabilisation. This will enable the individual sufficient time to readjust to living in the community and ensure symptom stabilisation before taking part in a study.
- Parents who have no regular contact with the index child or where there is known intention for their child to be removed.
- Parents who present with child protection of safeguarding issues.
- Parents seeking or receiving support from services regarding child management issues.
- Parents actively involved in other structured programmes.
Inclusion Criteria matched comparison group of parents for stage 1
The comparison group of parents will be matched for age, education, socioeconomic status and family composition where possible
- No previous history of psychotic illnesses.
- Primary parental caregiver for index child. This includes 10 hours of contact time with their child.
- Over 18 years of age.
- Have at least one child aged 3-10 years old.
- Identify difficulties in parenting during assessment.
- Proficient in written and spoken English.
- Capacity to provide informed consent.
Exclusion Criteria for comparison group
- Parents with schizophrenia-spectrum symptoms, diagnosis or history.
- Parents who have no regular contact with the index child or where there is known intention for their child to be removed.
- Parents seeking support from services regarding child management issues.
- Parents actively involved in other structured programmes.
- Parents/caregivers who do not have good working knowledge of English. They should have enough practical experience to be able to adequately use the English language to understand and respond to questions and to read and complete questionnaires.
- Insufficient language or cognitive ability to participant fully or provide informed consent.
Study Plan
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: Stage 2 Parents experiencing psychosis
Parents all receive the self-directed Triple P Positive Parenting Programme
|
10 week self-directed (guided) parenting intervention promoting self-belief, parenting confidence/self-efficacy and problem solving skills.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Positive and Negative Syndrome Scale (PANSS)
Time Frame: Initial Ax, Multiple Baseline Ax, Final Baseline Ax, 10 support sessions Ax, End Ax, Follow Up Ax. Ax from 0 - 16 weeks with 3 and 6 month follow up
|
Assessment of parental symptoms, mood, behaviours, aswell as social performance and depression
|
Initial Ax, Multiple Baseline Ax, Final Baseline Ax, 10 support sessions Ax, End Ax, Follow Up Ax. Ax from 0 - 16 weeks with 3 and 6 month follow up
|
|
Five Minute Speech Sample (FMSS)
Time Frame: Initial Ax, End Ax, Follow up Ax. Ax from 0 - 16 weeks with 3 and 6 month follow up
|
Assessment of Expressed Emotion using a 5 minute uninterrupted interview
|
Initial Ax, End Ax, Follow up Ax. Ax from 0 - 16 weeks with 3 and 6 month follow up
|
|
Modified Camberwell Family Interview (CFI)
Time Frame: Initial Ax only
|
In depth assessment of Expressed Emotion using a modified version of the CFI.
This version is for parents of well children.
|
Initial Ax only
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Depression, Anxiety and Stress Scale (DASS-21)
Time Frame: Initial Ax, Multiple Baseline Ax, Final Baseline Ax, 10 support sessions Ax, End Ax, Follow Up Ax. Ax from 0 - 16 weeks with 3 and 6 month follow up
|
Self-reported depression, anxiety and stress using a short form scale
|
Initial Ax, Multiple Baseline Ax, Final Baseline Ax, 10 support sessions Ax, End Ax, Follow Up Ax. Ax from 0 - 16 weeks with 3 and 6 month follow up
|
|
Warwick-Edinburgh Mental Well-being Scale (WEMWBS)
Time Frame: Initial Ax, Final Baseline Ax, End Ax, Follow Up Ax. Ax from 0 - 16 weeks with 3 and 6 month follow up
|
Self-reported general well-being
|
Initial Ax, Final Baseline Ax, End Ax, Follow Up Ax. Ax from 0 - 16 weeks with 3 and 6 month follow up
|
|
Eyberg Child Behaviour Inventory (ECBI)
Time Frame: Initial Ax, Final Baseline Ax, 10 support sessions Ax, End Ax, Follow Up Ax. Ax from 0 - 16 weeks with 3 and 6 month follow up
|
Parents self-reported child problem behaviour
|
Initial Ax, Final Baseline Ax, 10 support sessions Ax, End Ax, Follow Up Ax. Ax from 0 - 16 weeks with 3 and 6 month follow up
|
|
Strengths and Difficulties Questionnaire (SDQ)
Time Frame: Initial Ax, Final Baseline Ax, End Ax, Follow Up Ax. Ax from 0 - 16 weeks with 3 and 6 month follow up
|
Parents self-reported child behaviour assessing different aspects of behaviour, e.g.,: emotional symptoms, conduct problems, hyperactivity/inattention.
|
Initial Ax, Final Baseline Ax, End Ax, Follow Up Ax. Ax from 0 - 16 weeks with 3 and 6 month follow up
|
|
Parenting and Family Adjustment Scale (PAFAS)
Time Frame: Baseline, 1, 5, 10, follow up
|
An assessment of parenting skills and family relationships.
|
Baseline, 1, 5, 10, follow up
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Lauren Stockton, The University of Manchester
Study record dates
Study Major Dates
Study Start
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 15209: 15/NW/0532
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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