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Evaluation of a Clinical Transitional Program in Autism

Evaluation of a Clinical Program Specialized in the Diagnosis, Follow-up and Treatment of Young Adults With a Autism Spectrum Disorder: TAVA (Spanish Acronym for Support to Subjects With Autism in Their Transition to Adulthood)

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03392870
Acronym
TAVA
Enrollment
102
Registered
2018-01-08
Start date
2017-03-01
Completion date
2019-04-30
Last updated
2018-01-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Autism Spectrum Disorder (ASD)

Keywords

Autism Spectrum Disorder (ASD), Transition program

Brief summary

Clinical trial without drug, randomized: Comparison of a specific and integrative clinical protocol for young adults with autism to usual treatment. It will include both low and high-functioning participants.

Interventions

OTHERIntegrative interventional programme

The active condition includes specialized, multidisciplinary and intensive individual (weekly to monthly) or group interventions (weekly). Only high-functioning subjects will be considered for group interventions.

The control group will follow treatment as usual, consisting in conventional general psychiatrist/psychologist clinical follow-up. The frequency varies between 3-6 months or 15-21 days if worsening of symptoms or comorbid conditions.

Sponsors

Corporacion Parc Tauli
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Masking description

A researcher will be masked for group aleatorization (active, group) in order to unbiasedly evaluate outcomes which require subjective assesment of functionality.

Eligibility

Sex/Gender
ALL
Age
18 Years to 21 Years
Healthy volunteers
No

Inclusion criteria

* ASD diagnosis * Previous follow-up by child and adolescent psychiatry department at Corporació Sanitària Parc Taulí (CSPT)

Exclusion criteria

\- Living in a disabled residential setting

Design outcomes

Primary

MeasureTime frameDescription
Change in Quality of life.Baseline, 24 monthsThe World Health Organization Quality of Life (WHOQOL). Self-administered scale, quantitative. Spanish version.

Secondary

MeasureTime frameDescription
Change in: Depressive symptomsBaseline, 24 monthsBeck Depression Inventory-II (BDI-II) . Self-administered scale, quantitative.Spanish version.
Change in: Anxiety Symptoms.Baseline, 24 monthsBeck Anxiety Inventory (BAI). Self-administered scale, quantitative.Spanish version.
Change in: Obsessive-compulsive symptoms.Baseline, 24 monthsObsessive-Compulsive Inventory - Revised (OCI-R). Self-administered scale, quantitative. Spanish version.
Change in: ASD symptoms evaluated by parents/caregiver.Baseline, 24 monthsSocial Responsiveness Scale (SRS). Parents' self-administered scale, quantitative.Spanish version.
Change in: Asperger Symptoms.Baseline, 24 monthsAdult Asperger Assessment (AAA). Includes questionnaire (autism spectrum quotient, AQ) and (empathy quotient, EQ). Self-administered scale, quantitative.Spanish version.
Change in: Social phobia symptoms.Baseline, 24 monthsSocial Phobia Inventory (SPIN). Self-administered scale, quantitative. Spanish version.
Change in: Evaluation of support needs.Baseline, 24 monthsCamberwell Assessment of Need, revised (CAN-R). Administered by the professional, qualitative. Spanish version.
Change in: Caregiver's burden associated with the disorder.Baseline, 24 monthsThe Zarit Burden Interview. Caregiver self-report, quantitative. Spanish version.
Change in: Evaluation of the level of autonomy, self-regulation, self-empowerment, self-knowledge.Baseline, 24 monthsThe Arc's Self-Determination Scale. Self-administered scale. Spanish version. Quantitative.
Change in: ASD symptoms.Baseline, 24 monthsRitvo Autism Asperger's Diagnostic Scale (RAADS-R). Self-administered scale, quantitative. Spanish- translated version.

Countries

Spain

Contacts

Primary ContactESTHER VIA, PHD
evia@tauli.cat0034937240182
Backup ContactIsabel Parra, MD
iparra@tauli.cat937 23 10 10

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026