- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03916172
Evaluation of Psychological Intervention for Parents of Adolescents
Randomised Evaluation of Brief Psychological Intervention for Parents of Adolescents: The Open Door Approach to Parenting Teenagers (APT), in London, England
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
This study is the next step in the evaluation trajectory of the Open Door Approach to Parenting Teenagers (APT), and is a randomised controlled trial investigating whether receiving APT is more effective than being on a Waiting List (WL) in a sample of 60 parents of adolescents. We hypothesise that in comparison to those on the WL, those receiving APT will show significant improvements in:
- parental stress;
- parent-adolescent relationship;
- adolescent and parent wellbeing and mental health outcomes;
Secondary aims of the study will include:
- Ascertaining treatment fidelity
- Disseminating outcomes to inform policymakers, commissioners and providers, to facilitate evidence-based decisions about community services.
Procedure This trial will be carried out at two clinical sites in North London over 12months.
Method:
Parents and adolescents in the APT condition will be measured 3 times: at baseline, end-of-treatment, and follow-ups at three after the end-of-treatment. Those in WL will be measured three times from pre-treatment to three months follow-up. Then they will be offered APT. Measures are grouped into four batteries: for the parent, the adolescent, the therapist and an observer, and they will measure changes in parental stress, perceptions of the parent about their adolescent's psychopathology and relational problems, aspects of parenting relevant to aetiology and treatment of adolescent issues. The batteries also include variables mediating recovery, therapeutic alliance, health services utilisation and therapists' adherence to the ATP model.
Analysis plan:
The primary outcome will be analysed using within- and between-groups mean differences to estimate treatment effects. Results will be disseminated through scientific papers, academic conferences, the Open Door (OD) website, and reports will be distributed among educational and health institutions in our local network. If results have merit, the intervention manual will be published, and training will be offered to professionals outside OD. If successful, we anticipate this study to have a major impact on communities around the UK. It is a non-proprietary intervention that can be easily disseminated.
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
London, United Kingdom, N8 8PL
- Recruiting
- Open Door Young People's Consultation Service
-
Contact:
- Lara Taylor
- Phone Number: 02083485947
- Email: research@opendooronline.org
-
Contact:
- Alex Desiatnikov
- Phone Number: 020 8348 5947
- Email: research@opendooronline.org
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Being a parent of an adolescent aged 11-18 years
- Adolescent currently lives with parent for a minimum of 2 days/week
- Parent demonstrates clinically significant levels of concern on primary measure (Stress Index for Parents of Adolescents)
- Parent must be proficient in English so they may fully understand the material presented to them during the research study
Exclusion Criteria:
- Parent currently receiving treatment for psychotic illness
- Parent previously received APT intervention
- Adolescent has severe developmental disorder (e.g. Autism Spectrum Disorder) or serious life threatening health impairment
- Adolescent currently receiving individual psychotherapeutic treatment
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: APT Treatment
Participants in this arm will receive the Open Door Approach to Parenting Teenagers (APT).
It offers 6 weekly 50-minute appointments with an optional 7th review session.
|
APT works on a one-to-one or couple basis.
It offers 6 weekly 50-minute appointments with an optional 7th review session.
The practitioners delivering the intervention have qualifications in psychology, or significant experience of working with adolescent populations, and have undertaken training and supervision in the model.
Its aim is to help the parent manage the parenting of their teenager more effectively and establish a more balanced relationship by eliciting their views, feelings, and understanding of their teenager and their relationship, discussing their parental identity and role, carefully examining communication, responses, and information giving, and supporting appropriate boundary making.
This is achieved through a collaborative development of strategies, psychoeducation and behavioural experiments.
|
|
No Intervention: Waiting List
Participants in this group will be placed on a waiting list and will receive APT treatment after no longer than 25 weeks.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Stress Index for Parents of Adolescents (SIPA)
Time Frame: 5 months
|
This is a 112-item, self report that is structured into three main domain scores: Adolescent Domain (AD), Parent Domain (PD), and Adolescent-Parent Relationship Domain (APRD).
The AD has 4 subscale scores: Moodiness/Emotional Lability (MEL), Social Isolation/Withdrawal (ISO), Delinquency/Antisocial (DEL), and Failure to Achieve or Persevere (ACH).
The PD also has 4 subscale: Life Restrictions (LFR), Relationship with Spouse/Partner (REL), Social Alienation (SOC) and Incompetence/Guilt (INC).
The APRD has no subscales.
The Index of Total Parenting Stress (TPS) is a composite score computed from all items.
Scores are then classified into broad ranges: normal, borderline, clinically significant and clinically severe.
|
5 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Strengths And Difficulties Questionnaire Parent Version (SDQ-P)
Time Frame: 5 months
|
Strengths and Difficulties Questionnaires (SDQ): a brief, parent-report, behavioural questionnaire.
It comprises 25 items measuring emotional symptoms, conduct problems, hyperactivity/inattention, peer relationship problems and prosocial behaviour.
The measure has excellent psychometric properties, and national norms have been extracted from a large national survey of child and adolescent mental health carried out by the Office for National Statistics.
For all time-points except baseline, a follow-up version of the measure will be used, which adds questions regarding the intervention's impact.
|
5 months
|
|
Strengths and Difficulties Questionnaire Young Person Version (SDQ-YP)
Time Frame: 5 Months
|
Strengths and Difficulties Questionnaires (SDQ): a brief, self-report, behavioural questionnaire.
It comprises 25 items measuring emotional symptoms, conduct problems, hyperactivity/inattention, peer relationship problems and prosocial behaviour.
The measure has excellent psychometric properties, and national norms have been extracted from a large national survey of child and adolescent mental health carried out by the Office for National Statistics.
For all time-points except baseline, a follow-up version of the measure will be used, which adds questions regarding the intervention's impact.
|
5 Months
|
|
Alabama Parenting Questionnaire - Short Form (APQ-SF)
Time Frame: 5 months
|
A 12-item, self- report measure that focuses on parenting behaviours.
The parent APQ measures five dimensions of parenting that are relevant to the aetiology and treatment of child and adolescent problems: positive involvement with children, supervision and monitoring, use of positive discipline techniques, consistency in the use of such discipline and use of corporal punishment.
The APQ has good psychometric properties and has shown good discrimination between clinical and non-clinical groups.
|
5 months
|
|
Patient Health Questionnaire Module 9 (PHQ-9)
Time Frame: 5 months
|
A screen for depression, extensively used in the literature and clinical practice, with excellent psychometric properties.
|
5 months
|
|
Generalised Anxiety Disorder Screener (GAD-7)
Time Frame: 5 months
|
A 7-item screen with good sensitivity and specificity to capture and distinguish anxiety symptoms and disorders.
Extensively used in clinical and research contexts.
|
5 months
|
|
Alabama Parenting Questionnaire Young Person version (APQ-YP)
Time Frame: 5 months
|
This measure is complementary to the parent version described above.
It measures adolescents' perceptions about the parenting they receive.
|
5 months
|
|
EQ-5D-5L
Time Frame: 5 months
|
This is a standardised instrument developed by the EuroQol Group as a measure of health-related quality of life that can be used in a wide range of health conditions and treatments.
It consists of a descriptive system and the EQ Visual Analogue Scale (VAS).
The descriptive system comprises five dimensions: mobility, self-care, usual activities, pain/discomfort and anxiety/depression.
The EQ VAS records the patient's self-rated health on a vertical visual analogue scale.
The scores on these five dimensions can be presented as a health profile or can be converted to a single summary index number (utility) reflecting preferability compared to other health profiles.
|
5 months
|
|
Reflective Function Questionnaire (RFQ)
Time Frame: 5 months
|
A brief, easy-to-administer screening measure of reflective functioning.
It comprises 8 items yielding two sub-scales assessing certainty and uncertainty of mental states.
|
5 months
|
|
Conflict Behaviour Questionnaire (CBQ)
Time Frame: 5 months
|
A 20-item questionnaire that assesses perceived communication and conflict in the parent-adolescent relationship.
The CBQ has good psychometric properties and has been found to successfully discriminate between distressed and non-distressed families.
Both parent-report and self-report for adolescent versions will be used.
|
5 months
|
|
Parenting Scale (PS)
Time Frame: 5 months
|
This is a 30-item questionnaires that measures two dysfunctional discipline styles in parents: Laxness and Over-reactivity, and also measures verbosity.
This scale has good psychometric properties and has been found to discriminate between parents of clinic and non-clinic children.
|
5 months
|
|
Goal Based Measure
Time Frame: 5 months
|
Developed by the Child Outcomes Research Consortium.
Part of Open Door's regular practice.
It is a simple form that lists the patient's goals for the treatment, and every session the patient rates their accomplishment from zero to ten.
|
5 months
|
|
Working Alliance Inventory-Short Form-Client (WAI-SF-C)
Time Frame: 5 months
|
This measure will only be included in the end- of-treatment battery.
This is a 12 item questionnaire , which assesses three key aspects of the therapeutic alliance: (a) agreement on the tasks of therapy, (b) agreement on the goals of therapy and (c) development of an affective bond.
This brief measure has excellent psychometric properties.
|
5 months
|
|
Working Alliance Inventory-Short Form-Therapist (WAI-SF-T)
Time Frame: 5 months
|
The therapist counterpart for the measure listed above.
It will be completed by therapists at the end of treatment and is a 12-item scale that measures the alliance elements described above.
|
5 months
|
|
Working Alliance Inventory-Observer (WAI-O)
Time Frame: 5 months
|
The observer counterpart of the measure described above.
It is a 32-item scale that measures the alliance elements described above.
|
5 months
|
|
Experience of Services Questionnaire
Time Frame: 5 months
|
This measure will only be included in the end-of-treatment battery.
This is part of Open Door's regular practice.
The questionnaire addresses the quality of service provided: how well the intervention met the participants' needs, increased their skills, decreased the adolescent's problem behaviours, and whether the participants would recommend the program to others.
|
5 months
|
|
Adherence to the APT Model
Time Frame: 5 months
|
The APT manualised model includes checklists to be filled out by observers for each of the six sessions.
Only 1 session per participant will be scored and scoring will be performed by supervisors on a randomly selected intervention session's video.
These checklists contain both concrete actions the therapist must carry out during the selected session and elements regarding both the therapeutic stance, such as level of activity/passivity of the therapist.
|
5 months
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Alex Desiatnikov, Open Door Young People's Consultation Service
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 254697
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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.
Clinical Trials on Parent-Child Relations
-
University of LiegeActive, not recruitingParent-Child Relations | Child DevelopmentBelgium
-
McGill UniversitySave the Children; European Network of Foundations Children and Violence Evaluation... and other collaboratorsUnknown
-
University of CalgaryRecruitingParent-Child RelationsCanada
-
University of OttawaRecruitingParent-Child RelationsCanada
-
Universitätsklinikum Hamburg-EppendorfCompleted
-
Penn State UniversityActive, not recruiting
-
VISN 17 Center of ExcellenceUnited States Department of Defense; University of Texas at AustinEnrolling by invitation
-
University of AarhusCompletedParent-Child RelationsDenmark
-
Penn State UniversityCompleted
-
University of Wisconsin, MadisonLoyola University Chicago; Iowa State UniversityCompletedParent-Child Relations
Clinical Trials on The Open Door Approach to Parenting Teenagers (APT)
-
Sun Yat-Sen Memorial Hospital of Sun Yat-Sen UniversityGuangzhou First People's Hospital; The Third Affiliated Hospital of Southern... and other collaboratorsNot yet recruitingCervical Spondylotic Myelopathy
-
Misr International UniversitySuez Canal UniversityCompletedSinus Floor Augmentation | Maxillary Sinus | Alveolar Ridge AugmentationEgypt