Dyadic-based targeted prevention of maladaptive co-rumination and internalizing problems and disorders in Dutch early adolescent girls: A Cluster Randomized Controlled Trial on the effectiveness of the blended school-based mindfulness prevention program Happy Friends, Positive Minds.
- Conditions
- 10027946Internalizing symptoms and disorders (depression/anxiety)
- Registration Number
- NL-OMON55907
- Lead Sponsor
- Rotterdam University of Applied Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Not specified
- Target Recruitment
- 1000
To be eligible for inclusion, a participant/meisje must meet the following five
inclusion criteria:
(1) Aged 13 to age 15 years.
(2) Visiting a secondary school of Samenwerkingsverband Koers VO.
(3) Attending second or third grade of mainstream secondary education in
academic year 2023/2024.
(4) *Assigned female at birth, being a female transgender or being a nonbinary
adolescent.
(5) Having a mutual same gender (*assigned female at birth, being a female
transgender or being
a nonbinary adolescent) good or best friend at the same school.
To be eligible for inclusion, a dyad must meet the following inclusion
criterium:
(1) At least one of the two girls of one friendship dyad, or both girls, should
have a score of at least one standard deviation above the mean co-rumination
screening score on the Co-rumination Questionnaire Short (Hankin et al., 2010).
Exclusion criteria at the school level (to mitigate any risk of difficulties in
trial implementation):
(1) Not having a headteacher in academic year 2023/2024.
(2) Judged as 'inadequate* during most recent school inspection by the Dutch
Inspectorate of Education.
(3) Implementing another mindfulness-based intervention in academic year
2023/2024.
Exclusion criterium at the individual girl level:
(1) Following an/participating in an individual or group-based
mindfulness-based training in academic year 2023/2024.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method