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Study identifier: NCT05076214 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Aerobic Versus Leisure Group for Adolescents With Depression

Condition: Depressive Disorder, Major  ·  Sponsor: Lund University Hospital

PhaseNA
Planned participants122
Who can joinAll sexes, 13 Years to 17 Years
Healthy volunteersNo

About this study

The aim is to evaluate aerobic group exercise versus leisure group activities in adolescents with mild to moderate depression. Primary outcome is Children's Depression Rating Scale - Revised (CDRS-R). Secondary outcomes are Clinical Global Impressions - Severity and Improvement scales (CGI), self-reported Quick Inventory of Depression Symptomatology (QIDS- A17-SR), the self-reported Outcome Rating Scale (ORS), clinician rated Children Global Assessment Scale (C-GAS), aerobic capacity (VO2max), muscular strength, body, Body Mass Index (BMI), presence or activity of selected biological markers of neuroprotection and neuroinflammation in blood samples and a cost evaluation rated by parents with Trimbos/iMTA questionnaire for Costs associated with Psychiatric Illness - Child version (Tic-P) and the Child Health Utility (CHU9D) to facilitate estimation of Quality Adjusted Life Years. Further objectives are qualitative interviews to explore adolescents' experiences of the intervention as well as how their health and lifestyle are influenced and a validation of QIDS- A17-C and QIDS- A17-SR versus CDRS-R will be performed.

This description comes directly from the study's public registry record.

Talk to the study team

Håkan Jarbin, MD, PhD  ·  +46706778006  ·  hakan.jarbin@regionhalland.se

Rebecca Mortazavi, MD  ·  +46738011091  ·  rebecca.mortazavi@regionhalland.se

Always discuss trial participation with your own doctor first.

Locations (4)

Region HallandHalmstad, SwedenRecruiting
Prima Barn och vuxenpsykiatri AB (Stockholm-Handen)Stockholm, SwedenRecruiting
PRIMA Barn och vuxenpsykiatri AB (Stockholm-Järva)Stockholm, SwedenRecruiting
Region HallandVarberg, SwedenRecruiting

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Source record: clinicaltrials.gov/study/NCT05076214