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Trial registered on ANZCTR
Registration number
ACTRN12623000396628
Ethics application status
Approved
Date submitted
29/03/2023
Date registered
19/04/2023
Date last updated
7/04/2024
Date data sharing statement initially provided
19/04/2023
Type of registration
Prospectively registered
Titles & IDs
Public title
An evaluation of guided parent-delivered Cognitive Behaviour Therapy for children's perfectionism
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Scientific title
A randomised controlled feasibility trial of guided parent-delivered Cognitive Behaviour Therapy for children's perfectionism
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Secondary ID [1]
308709
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Nil
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Universal Trial Number (UTN)
U1111-1286-8492
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Trial acronym
STRATOSPHERIC
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Perfectionism
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depression
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eating disorders
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Condition category
Condition code
Mental Health
325653
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0
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Depression
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Mental Health
325654
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0
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Eating disorders
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Guided parent-delivered cognitive behaviour therapy for perfectionism (GPD-CBT-P) comprises of 6 sessions. Session 1 focuses on psychoeducation about the definition of perfectionism, exploring the difference between high standards and perfectionism, myths of the advantages of perfectionism and exploring reasons to change. The second session focuses on what keeps perfectionism going, examining typical unhelpful thinking patterns and behaviours that maintain perfectionism and how parental expectations and criticism can contribute to this. The third session focuses on setting up behavioural experiments with the children, to test out the truth or otherwise of their perfectionistic predictions and development of alternative beliefs. The fourth session focuses on psychoeducation about self-criticism, identifying the critical voice, identifying the compassionate voice, and involves parents asking their child to generate as many self-compassionate interpretations as possible for another child in a challenging hypothetical situation. The fifth session focuses on behaviours that can reinforce perfectionism, such as procrastination and checking, using problem solving. The sixth session focuses on the relationship between self-worth and achievement; identifying various factors that impact self-worth and to develop a program to expand those areas that are not linked to achievement. The content of the modules is drawn from the book "Overcoming perfectionism: A self-help guide using cognitive behavioural techniques". The content will be co-designed with parents in the first three months of the research to ensure that the content is suitably modified for use by parents with their children and has age-appropriate material. This co-design process will consist of a one-hour online focus group meeting, with up to 10 parents, where outcome will be decided by majority opinion. Over 6 sessions, delivered per parent dyad, both parents (where possible) will be guided through the content of the modules and encouraged to apply the content to themselves, as well as to instruct their children in the content they are learning. The guidance will be offered by trainee psychologists under expert supervision.
The approach is standardised yet can be flexibly delivered according to a families’ concerns, problems, and goals. Consistent with previous cost-effective online brief guided parent-delivered CBT for child anxiety, parents will be given a pdf of the intervention followed by six weekly online (remote) sessions with the trial guides, of up to 6 hours total contact. Each session will involve collaboratively setting an agenda for the session based on experience with the preceding week’s homework, current issues, and the module in focus. Participants will complete homework exercises to consolidate and practice the skills learnt during the session. To enable homework completion, worksheets will be prepared for the child with explanatory notes for the parents. Examples of homework include: completing a worksheet titled ‘Adam and Lucy’, which the child can complete with the parent to practise identifying perfectionism and how it is different to striving for high standards or excellence; completing the worksheet titled ‘Being Your Own Friend’, which the child can complete with the parent to practise using compassion for a fictional character, and then for themselves.
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Intervention code [1]
325766
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Prevention
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Comparator / control treatment
Wait list control group. Participants in the waitlist control will be informed of their status and will receive the pdf material at the end of 18 weeks.
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Control group
Active
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Outcomes
Primary outcome [1]
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For children we will use two subscales of the Almost Perfect Scale-Revised: High Standards (7 items) and Discrepancy (11 items). Items are rated on a 7-point scale ranging from 1 (strongly disagree) to 7 (strongly agree). High Standards is intended to assess adaptive and healthy striving while Discrepancy assesses the perception that personal high standards are not being met.
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Assessment method [1]
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Timepoint [1]
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18-weeks post-randomisation.
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Primary outcome [2]
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For parents we will use the 12-item Clinical Perfectionism Questionnaire, a self-report measure of clinical perfectionism developed to assess the impact of CBT-P. It has acceptable internal consistency and validity.
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Assessment method [2]
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Timepoint [2]
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18-weeks post-randomisation
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Primary outcome [3]
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Interest in study assessed by number of enquiries using audit of study enrolment data
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Assessment method [3]
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Timepoint [3]
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Assessed after enrolment of first 22 participants
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Secondary outcome [1]
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Perceived Stress Scale: Children. This 10-item measure is widely used for the early identification of children at risk of anxiety/stress. It is measured on a 4-point scale (Never to a Lot), with example items including: “How often do you feel worried about being too busy?”, “How often do you feel worried about your grades or school?”
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Assessment method [1]
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Timepoint [1]
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18-weeks post-randomisation
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Secondary outcome [2]
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Centre for Epidemiological Studies Depression Scale for Children. This 20-item self-report depression inventory is commonly used to measure depression in children. Each response to an item is scored as follows: 0 = “Not at All” 1 = “A Little” 2 = “Some” 3 = “A Lot”. Principal components analysis with children and adolescents identified three distinct factors: behavioral and cognitive components of depression and a happiness dimension.
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Assessment method [2]
420212
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Timepoint [2]
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18-weeks post-randomisation
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Secondary outcome [3]
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Body image and associated behaviours (e.g., My child compares their body negatively to others, My child feels nervous or uptight about their weight, My child follows strict rules about their eating, My child feels uptight or nervous about their body shape) using the Eating Disorder 15 items (ED15).
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Assessment method [3]
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Timepoint [3]
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18-weeks post-randomisation
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Secondary outcome [4]
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Satisfaction with school comprises six indicators, introduced by a question regarding the level of satisfaction: “How satisfied are you with each of the following things in your life?: Other children in your class?; Your school marks?; Your school experience?; Your life as a student?; Things you have learned?; and Your relationship with teachers?”. The response options were coded from 0 “Not at all satisfied” to 10 “Totally satisfied”.
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Assessment method [4]
420214
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Timepoint [4]
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18-weeks post-randomisation
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Secondary outcome [5]
420215
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8-item academic self-efficacy subscale (“How well do you succeed in finishing all your homework every day?”) from the Self-efficacy Questionnaire for Children
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Assessment method [5]
420215
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Timepoint [5]
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18-weeks post-randomisation
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Secondary outcome [6]
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number recruited into the trial (primary outcome) using audit of study enrolment
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Assessment method [6]
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Timepoint [6]
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Assessed after enrolment of first 22 participants
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Secondary outcome [7]
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number completing first assessment (primary outcome) using audit of study enrolment
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Assessment method [7]
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Timepoint [7]
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Assessed after enrolment of first 22 participants
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Secondary outcome [8]
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number randomised using audit of study enrolment
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Assessment method [8]
420627
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Timepoint [8]
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Assessed after enrolment of first 22 participants
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Secondary outcome [9]
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number retained in treatment (primary outcome) using audit of study enrolment
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Assessment method [9]
420628
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Timepoint [9]
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18-weeks post-randomisation
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Secondary outcome [10]
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number of completed assessments at each timepoint (primary outcome) using audit of study enrolment
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Assessment method [10]
420629
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Timepoint [10]
420629
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18-weeks post-randomisation
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Secondary outcome [11]
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percentage of homework tasks completed between sessions (primary outcome) using self-report
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Assessment method [11]
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Timepoint [11]
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18-weeks post-randomisation
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Secondary outcome [12]
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total hours of guidance used by each family (primary outcome) using therapist report
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Assessment method [12]
420631
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Timepoint [12]
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18-weeks post-randomisation
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Secondary outcome [13]
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treatment credibility, acceptability and effectiveness - self report using the Credibility Expectancy Questionnaire
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Assessment method [13]
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Timepoint [13]
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6-weeks post-randomisation
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Secondary outcome [14]
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Happiness - Happiness is assessed by asking: “Overall, how happy have you been feeling during the last two weeks?”, with response options from 0 “Not at all happy” to 10 “Totally happy”.
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Assessment method [14]
420636
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Timepoint [14]
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18-week post-randomisation
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Eligibility
Key inclusion criteria
The child is aged 7 to 12 years and the parents identify that their child has elevated perfectionism that causes problems to their psychosocial functioning. Questions will include: “Does your child set extremely high standards for themself? Do they chase these standards even if it leads to bad effects e.g., stress, low moods, anxiety, self-criticism, procrastination? Do they often feel disappointed after completing a task because they feel they could have done better?”. Our previous work has shown self-identification of perfectionism results in 72% of participants scoring at least one standard deviation above published norms on the Frost Concern over Mistakes subscale.
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Minimum age
7
Years
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Maximum age
No limit
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
Receiving other psychological services for perfectionism while participating in the trial.
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Study design
Purpose of the study
Prevention
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Randomisation will be achieved using computer-generated (http://www.jerrydallal.com/random/randomize.htm), quasi-random numbers and will be conducted by an independent researcher not associated with the research. Once generated, this information is passed to the project coordinator.
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Stratified allocation - eligible families will be stratified according to scores on the Discrepancy scale of the Almost Perfect Scale – Revised. Male children scoring greater than or equal to 46.9 and female children scoring greater than or equal to 48.6 will be assigned as having high discrepancy and children under these cut off scores will be assigned as having low discrepancy.
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Masking / blinding
Open (masking not used)
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Who is / are masked / blinded?
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Intervention assignment
Parallel
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Other design features
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Phase
Not Applicable
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Type of endpoint/s
Efficacy
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Statistical methods / analysis
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Recruitment
Recruitment status
Recruiting
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Date of first participant enrolment
Anticipated
3/07/2023
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Actual
13/11/2023
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Date of last participant enrolment
Anticipated
28/06/2024
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Actual
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Date of last data collection
Anticipated
31/10/2024
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Actual
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Sample size
Target
66
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Accrual to date
21
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Final
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Recruitment in Australia
Recruitment state(s)
SA,WA
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Funding & Sponsors
Funding source category [1]
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Charities/Societies/Foundations
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Name [1]
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Channel 7 Children’s Research Foundation
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Address [1]
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PO Box 2438
Regency Park SA 5010
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Country [1]
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Australia
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Primary sponsor type
University
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Name
Flinders University
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Address
GPO Box 2100, Adelaide, SA, 5001
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Country
Australia
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Secondary sponsor category [1]
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Individual
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Name [1]
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Tracey Wade
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Address [1]
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Flinders University
GPO Box 2100, Adelaide, SA, 5001
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Country [1]
315312
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Australia
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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Flinders University Human Research Ethics Committee
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Ethics committee address [1]
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Flinders University, GPO Box 2100, Adelaide, SA, 5001
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Ethics committee country [1]
312205
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Australia
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Date submitted for ethics approval [1]
312205
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16/11/2022
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Approval date [1]
312205
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22/12/2022
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Ethics approval number [1]
312205
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5816
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Summary
Brief summary
We aim to examine the feasibility of a new guided parent-delivered CBT-P (GPD-CBT-P) whose child is aged between 7 and 12 years of age in terms of recruitment through educational settings and retention rates. In addition, we will gather data how GPD-CBT-P performs against waitlist control for change over 18-weeks post-randomisation on self-report (parent and child) measures of perfectionism, stress, depressive symptoms, and body image disturbance. In addition, this will be the first occasion that academic outcomes (satisfaction and self-efficacy) will be examined in a randomised controlled trial design. This is a feasibility trial that will provide a plausible range of point estimates of the efficacy of GPD-CBT-P on standardised continuous symptom measures for our secondary aim. In this way, we can refine the treatment manual and contribute to the design. As a feasibility study we do not pose hypotheses but will examine our primary outcomes (number of enquiries, number recruited into the trial, number completing first assessment, number randomised, number retained in treatment, number of completed assessments at each timepoint, percentage of homework tasks completed between sessions, total hours of guidance used by each family), as well as the perceived treatment credibility, acceptability and effectiveness, and the between group effect sizes (95% confidence intervals) for our measures.
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Prof Tracey Wade
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Address
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Flinders University,
GPO Box 2100, Adelaide, SA 5001
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Country
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Australia
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Phone
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+61 882013736
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Fax
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+61882013877
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Email
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[email protected]
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Contact person for public queries
Name
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Tracey Wade
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Address
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Flinders University,
GPO Box 2100, Adelaide, SA 5001
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Country
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Australia
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Phone
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+61 882013736
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Fax
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+61882013877
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Email
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[email protected]
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Contact person for scientific queries
Name
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Tracey Wade
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Address
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Flinders University,
GPO Box 2100, Adelaide, SA 5001
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Country
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Australia
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Phone
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+61 882013736
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Fax
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+61882013877
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Email
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[email protected]
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Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
Yes
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What data in particular will be shared?
All of the individual participant data collected during the trial, after de-identification
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When will data be available (start and end dates)?
January 2025, no end date determined
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Available to whom?
Other researchers
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Available for what types of analyses?
Meta-analyses and replication analyses
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How or where can data be obtained?
Tracey Wade's Open Science Framework site: https://osf.io/rtzv3/
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What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
No additional documents have been identified.
Download to PDF