Skip to main content
Clinical Trials/NCT02622048
NCT02622048
Unknown
Not Applicable

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

University of Manchester1 site in 1 country60 target enrollmentSeptember 2015

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Parenting
Sponsor
University of Manchester
Enrollment
60
Locations
1
Primary Endpoint
Positive and Negative Syndrome Scale (PANSS)
Last Updated
9 years ago

Overview

Brief Summary

The purpose of this trial is to explore parent-child interactions in parents with and without psychosis, and ascertain whether a brief (10 week) supported self-help parenting program offered to parents in their own homes can help improve parents' self-efficacy and general well-being, as well as interpretations of their parent-child relationship and child behaviour in children who are 3-10 years old.

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.

Registry
clinicaltrials.gov
Start Date
September 2015
End Date
July 2017
Last Updated
9 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Lauren Stockton

PhD Clinical Psychology Student

University of Manchester

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

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

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

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.

Secondary Outcomes

  • Depression, Anxiety and Stress Scale (DASS-21)(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)(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)(Baseline, 1, 5, 10, follow up)
  • Eyberg Child Behaviour Inventory (ECBI)(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)(Initial Ax, Final Baseline Ax, End Ax, Follow Up Ax. Ax from 0 - 16 weeks with 3 and 6 month follow up)

Study Sites (1)

Loading locations...

Similar Trials