The effectiveness of a manualized cognitive-behavioral treatment (CBT) for clinically anxious children will be tested in a sample of Dutch children (aged 8-12 years) who are assigned to one of three Dutch community agencies in Arnhem and Nijmegen.…
ID
Bron
Aandoening
Anxiety, anxiety disorders, children, childhood anxiety, mother-child interaction, parent-child interaction, therapeutic alliance
Angst, angststoornissen, kinderen, moeder-kind interactie, ouder-kind interactie, therapeutische relatie
Ondersteuning
Pro Persona Youth
Ambulatorium Nijmegen
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
1. Anxiety symptom levels on the SCARED;<br>
2. Internalizing problems on the CBCL/TRF;<br>
3. Diagnoses based on the DAWBA.
Achtergrond van het onderzoek
The present project aims to examine variations in effectiveness of cognitive-behavioral therapy in clinically anxious children. The effectiveness of a manualized cognitive-behavioral treatment for childhood anxiety disorders will be compared with treatment as usual within community agencies. It is expected that the manualized cognitive-behavioral treatment will provide less anxiety symptoms after treatment and at follow-up compared to treatment as usual.
Doel van het onderzoek
The effectiveness of a manualized cognitive-behavioral treatment (CBT) for clinically anxious children will be tested in a sample of Dutch children (aged 8-12 years) who are assigned to one of three Dutch community agencies in Arnhem and Nijmegen. It is expected that children who receive the manualized treatment will show lower levels of anxiety symptoms compared to the control group, which will receive treatment as usual by the institutions.
Onderzoeksopzet
1. Baseline;
2. Posttreatment (3 months after intervention);
3. Follow-up (after 1 year).
Onderzoeksproduct en/of interventie
Children will be randomly assigned to the experimental or control group.
Children in the experimental group will receive a manualized cognitive behavioral treatment for anxiety disorders developed and tested by Bogels and colleagues (Bodden et al., 2008).
Children in the control group will receive treatment as usual in the institution for the same period of time (12-15 weeks).
Publiek
Postbus 9104
M.E.M. Doorn, van
Nijmegen 6500 HE
The Netherlands
+31 (0)24 3612812
m.vandoorn@pwo.ru.nl
Wetenschappelijk
Postbus 9104
M.E.M. Doorn, van
Nijmegen 6500 HE
The Netherlands
+31 (0)24 3612812
m.vandoorn@pwo.ru.nl
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
Children between the age of 8 and 12 with:
1. General anxiety disorder;
2. Seperation anxiety disorder;
3. Social anxiety disorder;
4. Anxiety disorder NOS.
Above the cutt-off score of the short version of the SCARED.
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
Children with:
1. Specific phobia;
2. Obsessive compulsive disorder;
3. Post traumatic stress disorder;
4. Autism;
5. IQ below 80.
Opzet
Deelname
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 | NL2826 |
| NTR-old | NTR2967 |
| Ander register | METC Radboud University Nijmegen : ECG16122010 |
| ISRCTN | ISRCTN wordt niet meer aangevraagd. |