CompletedNot Applicable

Super Skills for Life Effectiveness in the Online Modality

Spain30 participantsStarted 2017-10-01

Plain-language summary

The study aims to evaluate the effectiveness of the transdiagnostic program Super Skills for Life (SSL). This protocol targets children aged 8 to 12 with emotional problems (anxiety, depression, low self-esteem, and lack of social skills). SSL consists of eight sessions targeting common risk factors for internalizing disorders such as cognitive distortions, avoidance, emotional management, low self-esteem, social skills deficits, and coping strategies. The present research focuses on assessing the effectiveness of SSL applied online (through a virtual platform).

Who can participate

Age range8 Years – 12 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Children aged 8-12 * Presenting subclinical symptoms of emotional problems (anxiety, depression) * Speaking, reading, writing, and understanding Spanish. * Not receiving psychological or pharmacological treatment for emotional and/or behavioral problems Exclusion Criteria: * Had a psychiatric diagnosis already established * Presenting a severe developmental disorder (intellectual disability, autism spectrum disorder, etc).

What they're measuring

Change from baseline depression symptoms to immediately after the intervention

Timeframe: 1 year after the intervention

Depression symptoms at 1 year

Timeframe: 1 year after the intervention

Change from baseline parent-reported depression to immediately after the intervention

Timeframe: baseline and immediately after the intervention

Parent-reported depression at 1 year

Timeframe: 1 year after the intervention

Change from baseline children's reported anxiety symptoms to immediately after the intervention

Timeframe: baseline and immediately after the intervention

Change from baseline parent-reported anxiety symptoms to immediately after the intervention

Timeframe: baseline and immediately after the intervention

Children's reported anxiety symptoms at 1 year

Timeframe: 1 year after the intervention

Trial details

NCT IDNCT05589090

SponsorUniversidad Miguel Hernandez de Elche

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2022-12-01

View on ClinicalTrials.gov More Depressive Disorder trials

Plain-language summary

Who can participate

Age range8 Years – 12 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

What they're measuring

Change from baseline depression symptoms to immediately after the intervention

Timeframe: 1 year after the intervention

Depression symptoms at 1 year

Timeframe: 1 year after the intervention

Change from baseline parent-reported depression to immediately after the intervention

Timeframe: baseline and immediately after the intervention

Parent-reported depression at 1 year

Timeframe: 1 year after the intervention

Change from baseline children's reported anxiety symptoms to immediately after the intervention

Timeframe: baseline and immediately after the intervention

Change from baseline parent-reported anxiety symptoms to immediately after the intervention

Timeframe: baseline and immediately after the intervention

Children's reported anxiety symptoms at 1 year

Timeframe: 1 year after the intervention