- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05473104
PEERS® for Italy, a Study on Social Skills Intervention for Adolescents With Autism Spectrum Disorder (ASD).
July 21, 2022 updated by: Laura Maria Fatta, Istituto Superiore di Sanità
Program for the Education and Enrichment of Relational Skills (PEERS®) for Italy. A RCT's Study on Social Skills Intervention for Adolescents With Autism Spectrum Disorder (ASD).
TThe research aims to verify the Italian adaptation of a parent-mediated group training focused on social skills for adolescents with autism spectrum disorder (ASD).
The Program for the Education and Enrichment of Relational Skills PEERS® is an evidence-based program with substantial literature (over 40 studies) applied in several countries.
For the present study, about 40 adolescents, both boys, and girls with ASD, are enrolled and randomized into two groups.
Groups (experimental group and waiting list) took part in the Italian telehealth adaptation of PEERS® at different times and were evaluated at several time points (baseline, pre-treatment, post-treatment, and follow-up).
The objective of the comparison was to explore the primary outcomes, such as the impact of training on social knowledge and performance, and secondary outcomes, like psychiatric comorbidities and neuropsychological profile.
The hypothesis is that social skills (knowledge and performance) improve after training in the experimental group and affect the secondary outcomes, and the achievements are maintained at 3-months follow-up.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
37
Phase
- Phase 2
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Rome
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Roma, Rome, Italy, 00161
- Istituto Superiore di Sanità
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
12 years to 18 years (Child, Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- a previous and current diagnosis of ASD, by a clinical team, according to DSM-5, clinical observation and structured assessment with standardized tests (Autism Diagnostic Observation Schedule- Second Edition; ADOS-2; Lord et al., 2012)
- Verbal Comprehension Index scores at least 80 on the Italian version of the WISC-IV scale (Orsini et al.,2012).
- Chronological age between 12 and 18 years;
- Social problems as reported both by the parents and adolescents;
- Italian fluency for the adolescent and parent
- Abstention from other social skills training (following a manualized protocol).
- No history of adolescent major mental illness, such as bipolar disorder, schizophrenia, or psychosis;
- No history of hearing, visual, or physical impairmentsExclusion Criteria:
Exclusion Criteria:
- No diagnosis of ASD.
- IQ Total score below 70 or Verbal Comprehension Index scores below 80 on the Italian version of the WISC-IV scale (Orsini et al.,2012).
- Lack of motivation (both parents or adolescents).
- Participation in another social skills training (following a manualized protocol).
- Auto-aggressive behaviors
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: experimental group
Teens and parents participate in the training once a week for 14 consecutive weeks in parallel groups.
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Social training targeting adolescents with ASD and focused on making and keeping friends
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No Intervention: waiting-list group
Teens and parents participate in the training in a second moment, immediately after the experimental group concluded the program, once a week for 14 consecutive weeks in parallel groups.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Social Responsiveness Scale (SRS) (Costantino & Gruber, 2005), changes after 14 weeks and 3 months.
Time Frame: pre-treatment, after 14 weeks and 3 months after the start of training (within two weeks)
|
is a quantitative measure completed by caregivers and teachers, consisting of 65 items, assessing symptoms characteristic of autism spectrum disorders, in children and adolescents aged 4 to 18 years.
In this study it is used as a primary outcome measure to assess global social skills.
|
pre-treatment, after 14 weeks and 3 months after the start of training (within two weeks)
|
|
Quality of Socialization Questionnaire-Revised (QSQ-R) (Laugeson & Frankel, 2010; Laugeson et al., 2012), changes after 14 weeks and 3 months.
Time Frame: pre-treatment, after 14 weeks and 3 months after the start of training (within two weeks)
|
It is a social performance measure filled out both by caregivers and adolescents, assessing, through numbers and quality of get-togethers, the ability to know how to make and maintain friendships in the natural contexts of adolescents.
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pre-treatment, after 14 weeks and 3 months after the start of training (within two weeks)
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|
Test of Adolescent Social Skills Knowledge (TASSK) (Laugeson & Frankel 2010), changes after 14 weeks and 3 months.
Time Frame: pre-treatment, after 14 weeks and 3 months after the start of training (within two weeks)
|
It is a 30-question questionnaire completed by adolescents to monitor the acquisition of the topics covered within the PEERS®.
It is used to evaluate social knowledge.assessing,
through numbers and quality of get-togethers, the ability to know how to make and maintain friendships in the natural contexts of adolescents.
|
pre-treatment, after 14 weeks and 3 months after the start of training (within two weeks)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Child Behavior Checklist (CBCL) (Achenbach & Rescorla, 2001), changes after 14 weeks and 3 months.
Time Frame: pre-treatment, after 14 weeks and 3 months after the start of training (within two weeks)
|
CBCL is widely used to evaluate developmental psychopathology through scales that assess specific dimensions (Anxiety/Depression; Withdrawal/Depression; Somatic Complaints; Social Problems; Thinking Problems; Attention Problems; Rule-Breaking Behaviors; Aggressive Behaviors), general (Internalizing, Externalizing, and Total Problems), emotional-behavioral problems according to some of the DSM diagnostic categories (Affective Problems; Anxiety Problems; Somatic Problems; Attention-Deficit/Hyperactivity Problems; Oppositional-Provocative Problems; Conduct Problems).
We used parent, teacher, and adolescent forms
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pre-treatment, after 14 weeks and 3 months after the start of training (within two weeks)
|
|
Multidimensional Anxiety Scale for Children-Second Edition (MASC-2) (March, 2013), changes after 14 weeks and 3 months.
Time Frame: pre-treatment, after 14 weeks and 3 months after the start of training (within two weeks)
|
It is a 50-item questionnaire completed by adolescents, assessing anxiety in children and adolescents from 8 to 19 years of age comprehensively.
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pre-treatment, after 14 weeks and 3 months after the start of training (within two weeks)
|
|
Children's Depression Inventory, Second Edition (CDI-2) (Kovacs, 2010), changes after 14 weeks and 3 months.
Time Frame: pre-treatment, after 14 weeks and 3 months after the start of training (within two weeks)
|
It is a comprehensive, multi-perspective assessment of depressive symptoms in children and adolescents aged 7 to 17 years that allows early identification of depressive symptoms and provides an index of their extent and severity.
We used the children and adolescent version
|
pre-treatment, after 14 weeks and 3 months after the start of training (within two weeks)
|
|
Behavior Rating Inventory of Executive Function, Second Edition (BRIEF-2) (Gioia et al., 2015), changes after 14 weeks and 3 months.
Time Frame: pre-treatment, after 14 weeks and 3 months after the start of training (within two weeks)
|
ICompleted by caregivers, assessing the executive functioning profile of children between the ages of 5 and 18 years oldand adolescents aged 7 to 17 years that allows early identification of depressive symptoms and provides an index of their extent and severity.
We used the children and adolescent version
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pre-treatment, after 14 weeks and 3 months after the start of training (within two weeks)
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Autism Quotient (AQ) (Baron-Cohen et al., 2001)
Time Frame: pre-treatment (within two weeks)
|
It was administered to parents separately to evaluate autism traits.
|
pre-treatment (within two weeks)
|
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Adaptive Behavior Assessment System - Second Edition (ABAS-II) (Harrison & Oakland 2003)
Time Frame: pre-treatment (within two weeks)
|
It is a rating scale that measures daily living skills.
It can detect these skills in individuals aged 0-89 years.
For the present study, the caregivers' form was used to assess the behavior of people aged 5 to 21.
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pre-treatment (within two weeks)
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Social validity
Time Frame: post-treatment (within two weeks)
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The questionnaire was administered to adolescents, and caregivers to evaluate the usefulness of the program sessions (using a 3-point likert scale) and whether they would recommend the training to other families/peers.
Finally, they were asked to indicate 3 strengths and 3 weaknesses.
The questionnaires were constructed specifically for the current research project from a reworking of a form found in another study that used PEERS® to test the program's effectiveness with participants with Turner Syndrome (Wolstencroft et al., 2018).
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post-treatment (within two weeks)
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
January 14, 2021
Primary Completion (Actual)
April 14, 2021
Study Completion (Actual)
November 14, 2021
Study Registration Dates
First Submitted
July 4, 2022
First Submitted That Met QC Criteria
July 21, 2022
First Posted (Actual)
July 25, 2022
Study Record Updates
Last Update Posted (Actual)
July 25, 2022
Last Update Submitted That Met QC Criteria
July 21, 2022
Last Verified
July 1, 2022
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 871
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
No
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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