- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06159738
Parental Cognitions and Children's Wellbeing
November 28, 2023 updated by: University of Edinburgh
The Role of Parental Cognitions in Predicting Wellbeing in Adolescence
The current study aims to address the research limitations in previous studies by adopting a longitudinal design to investigate the associations between parental cognitions (parental expectations, parental beliefs, and parental attributional styles) and adolescents' wellbeing, resilience, and coping strategies across an extended period.
Two main research questions were posed: 1) What are the associations between parental cognition factors (parental attribution, parental expectations, and parental beliefs and adolescents' outcomes (wellbeing, resilience, and stress-coping)?
2) Which parental cognition factor has the highest probability in predicting the changes of adolescents' wellbeing, resilience, and coping strategies over time?
To answer these research questions, bayesian regression analysis was used to identify the best fitting model of adolescents' wellbeing outcomes and to discern the risk and protective roles of parental cognition factors within the model.
Bayesian regression approach also enables the assignment of probabilities to each parental cognition factor, quantifying their credibly in relation to adolescents' wellbeing outcomes.
Study Overview
Status
Completed
Conditions
Detailed Description
93 parents who has an adolescent aged between 11 to 16 years old were recruited.
Only 65 of them had their adolescents to agree to sign up.
This result in a 65 dyads of parents and adolescents in total.
Parents and adolescents completed the measures on Qualtrics online survey site, respectively.
After completion, researcher contacted parents to arrange a zoom call/phone call with their adolescents to complete measures on wellbeing and perceived stress.
Among 93 parents who signed up the research, only 65 of their adolescents managed to complete both the online questionnaire and the call with the researcher at baseline.
Six months after baseline, only adolescents were asked to repeat the above procedures as the follow-up.
37 adolescents completed the follow-up procedure, which makes this study sample ended up with 37 dyads of parents and adolescents.
The primary objective of this observational study is to determine which parental factor, among the three primary parental cognition schemas (parental expectations, parental beliefs, and parental attributional styles), exhibits consistent effects on predicting the changes of adolescents' wellbeing over time.
Study Type
Observational
Enrollment (Actual)
90
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
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Edinburgh, United Kingdom, EH16 4TJ
- The University of Edinburgh
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-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
Yes
Sampling Method
Probability Sample
Study Population
93 parents who has an adolescent aged between 11 to 16 years old were recruited.
Only 65 of them had their adolescents to agree to sign up.
This result in a 65 dyads of parents and adolescents in total.
39 of them were recruited through secondary state schools, primary state schools, and independent schools in Scotland, England, and Ireland.
15 participants were recruited through a Parent Webinar hosted by the research team.
6 participants were recruited from parenting and child organisations (Glasgow City Parents Group, Shared Parenting Scotland, Connect Scotland, Parental Minds, and the LUNA Project).
5 participants were recruited through research social account on Facebook and Twitter.
Description
Inclusion Criteria:
- Criteria for participation were parents and their adolescents aged 11 to 16 years old who have no neurodevelopmental conditions reported by parents (specifically to developmental disorders that may include learning difficulties, such as ASD, ADHD, and intellectual disability).
Exclusion Criteria:
- Adolescents with neurodevelopmental disorders, adolescents aged younger than 11 years old or older than 16 years old, and adolescents and parents who are not fluent in English will also be excluded as the measurements in this study are written in English.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Wellbeing
Time Frame: 6 months
|
Adolescents' wellbeing (quality of life) measured by KIDCSREEN-27
|
6 months
|
|
Resilience
Time Frame: 6 months
|
Adolescents' trait resilience measured by Conner Davidson Resilience Scale
|
6 months
|
|
Coping Styles
Time Frame: 6 months
|
Adolescents' coping styles measured by Brief Coping Scale
|
6 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Hungtzu Tai, University of Edinburgh
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
October 31, 2021
Primary Completion (Actual)
November 15, 2023
Study Completion (Actual)
November 15, 2023
Study Registration Dates
First Submitted
November 28, 2023
First Submitted That Met QC Criteria
November 28, 2023
First Posted (Estimated)
December 7, 2023
Study Record Updates
Last Update Posted (Estimated)
December 7, 2023
Last Update Submitted That Met QC Criteria
November 28, 2023
Last Verified
November 1, 2023
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- AC21089
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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