Fundació Institut de Recerca de lHospital de la Santa Creu i Sant Pau
Barcelona, Catalonia, 08041, Spain
Location status: Recruiting
Location contact
Júlia Carrasco, Mrs.
CONTACT
Maria J Portella, Dr.
CONTACT
NCT Number: NCT07041502
Currently, many autistic youths struggle to adapt to academic programs or the workforce, often turning to third-sector organizations such as specialized associations and foundations. This may be due to factors such as emotional dysregulation and executive dysfunction, which interfere with their psychosocial adaptation abilities, leading to anxiety and depression. These challenges have a neurobiological basis tied to the unique complexities of the autistic brain, which experiences emotional and cognitive overload and lacks attentional filters. To address this issue, the emotional and executive functioning of autistic youths at the Friends Foundation will be assessed through objective and subjective assessments.
This data collection will serve as a foundation for conceptualizing and co-creating a more realistic affective-cognitive remediation program, integrating user perspectives (conceptualization of interventions for systematic implementation). The program aims to improve the socio-occupational and emotional adaptation difficulties that often contribute to mental health challenges within this underserved population. It is important to highlight that many existing programs focus on cognitive training and social skills, neglecting strategies for adaptation and emotional regulation. This project will stand out for its inclusive design, featuring a representative sample of both sexes, overcoming the usual limitation of male-centered approaches.
Interested in participating?
Request Info16 year–30 year
All sexes
Observational
Barcelona, Catalonia, 08041, Spain
Location status: Recruiting
Júlia Carrasco, Mrs.
CONTACT
Maria J Portella, Dr.
CONTACT
The mixed or hybrid sequential study design (quantitative → qualitative → quantitative) includes three parts:
A) Assessment of socio-occupational, neuropsychological, and psychological variables to establish relationships between the degree of impairment and socio-occupational integration. Quantitative study.
B) Focus groups to determine the contents of the intervention program, which will be co-created as the Aut-CARE program. Qualitative study.
C) Pilot study of the Aut-CARE program to evaluate its format, content, feasibility, and acceptability.
Individuals aged 16 to 30 years with an ASD diagnosis, levels 1 and 2. The calculated sample size is 37 subjects for sub-study A; the minimum sample size for the focus groups (sub-study B) is 14; and a maximum of 10 participants for the pilot study (sub-study C).
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
There is no intervention
Time frame: 1 day
The DERS is a measure of emotional dysregulation. The raw scores range from 36 to 180. Higher scores mean more difficulties.
Time frame: 1 day
A set of neuropsychological tests is administered: Trail Making Test-A, Trail Making Test-B, Digit Symbol Substitution Test, Digit Span, Letter and Numbers, and Phonetic Fluency (PMR). Scores will be t-transformed (mean=50, SD=10), so high scores mean better performance.
Contact information is provided by the study sponsor or research team.
Alejandra Espinosa
CONTACT
Muriel Vicent-Gil, Dr
CONTACT
Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau
Other
Co-creation of the Aut-CARE Intervention to Improve the Cognitive and Emotional Functioning of Young Adults on the Autism Spectrum and Facilitate Their Socio-occupational Integration
Acronym: Aut-CARE
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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