The effectiveness of an indicated indicated depression and anxiety prevention program ('Een Sprong Vooruit') will be tested in a Dutch sample of adolescents (aged 11-15) with high familial risk. It is expected that the adolescents who…
ID
Bron
Aandoening
Prevention, depression, anxiety, adolescents, parental psychopathology
Ondersteuning
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
1. Depression;<br>
Achtergrond van het onderzoek
In this randomized controlled trial (RCT with 2 conditions, intervention and control group) the effectiveness of an indicated and selective prevention program aimed at depression and anxiety for adolescents (aged 11-15) with high familial risk will be tested. Adolescents in the intervention condition receive the program consisting of the 6 sessions of 90 minutes that will be implemented at school. Measurements of primary and secondary outcomes will be conducted in the intervention and control group at baseline, immediately after each session 2, 4 and 6 (post-intervention), at 6 months and 12 months follow-up.
Doel van het onderzoek
The effectiveness of an indicated indicated depression and anxiety prevention program ('Een Sprong Vooruit') will be tested in a Dutch sample of adolescents (aged 11-15) with high familial risk. It is expected that the adolescents who receive the intervention will show lower levels of depressive and anxiety symptoms during follow-up, compared to the control group.
Onderzoeksopzet
1. Baseline;
2. Intervention phase 1 (after session 2);
3. Intervention phase 2 (after session 4);
4. Post-intervention (after session 6);
5. Follow-up 1 (6 months);
6. Follow-up 2 (12 months).
Onderzoeksproduct en/of interventie
The children with symptoms of depression and/or anxiety and with parents with elevated levels of depression and/or anxiety randomly assigned to the intervention or control condition. Participants in the intervention condition receive the program, consisting of 6 sessions of 90 minutes that will be implemented at school. Participants in the intervention and participants in the control condition will fill in questionnaires at six moments during the study. After the study, adolescents in the control condition will also get the chance to follow the lessons.
Algemeen / deelnemers
Wetenschappers
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
- adolescent is aged between 11-15 years old;
- shows increased levels of depression and or anxiety;
- at least one of the parents shows symptoms of a depression or anxiety disorder;
- both adolescent and parents have sufficient knowledge of the Dutch language
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
- absence of parental permission;
- adolescent already receives treatment for mental health problems
- presence of prominent suicide ideation (score of 2 CDI 2 suicide item)
Opzet
Deelname
Voornemen beschikbaar stellen Individuele Patiënten Data (IPD)
Opgevolgd door onderstaande (mogelijk meer actuele) registratie
Geen registraties gevonden.
Andere (mogelijk minder actuele) registraties in dit register
Geen registraties gevonden.
In overige registers
Register | ID |
---|---|
NTR-new | NL3563 |
NTR-old | NTR3720 |
Ander register | - : - |
ISRCTN | ISRCTN wordt niet meer aangevraagd. |