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Not yet recruitingNCT07830160Updated Sep 21, 2026

Improving Autism Program Quality in Special Education Units: The Use of an APERS-based Model to Support Student Learning and Participation

An interventional study of APERS+ in Autism and Sociocommunicative Challenges, sponsored by Stockholm University. Not yet recruiting at 1 site in Sweden. Open to participants aged 5 Years to 13 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-09-21.

Sponsored by Stockholm University · Not applicable, Interventional, and Other

Phase
Not applicable
Study type
Interventional
Enrollment
200
Allocation
Non-randomized
Ages
5 Years to 13 Years
Sex
All
01

Study summary

This study assesses the effect of using the Autism Program Environment Rating Scale (APERS) as a tool for providing feedback, in-service training, and coaching to school staff in order to improve program quality in special education units (SEUs) for children with autism or related sociocommunicative challenges (SCCs). APERS is used in its culturally validated Swedish version (APERS-Primary-SE). Using a quasi-randomized parallel-group design, SEUs will be allocated to either an experimental (APERS+) or control (TAU) condition. In the APERS+ condition, school staff receive continuous and systematic feedback provided by trained coaches based on the initial APERS assessment. In the TAU condition, schools will also receive feedback based on the initial APERS assessment, but no continuous coaching.

It is hypothesized that the APERS based intervention will improve overall program quality for children with autism or related SCCs as compared to TAU. Additionally, we also expect the intervention to improve student functioning, students' individual goal attainment, students' perception of their schools, and teacher self-efficacy as compared to TAU.

02

Conditions studied

  • Autism
  • Sociocommunicative Challenges

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03

In context

Autistic Disorder

1,030 studies on the registry are indexed under Autistic Disorder; 266 are open to participants now.

This study's planned enrollment of 200 is above the median of 49 across 811 interventional studies indexed under Autistic Disorder.

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Lead sponsor

Stockholm University is the lead sponsor of 25 studies on the registry; 2 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
5 Years to 13 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Eligibility criteria

Inclusion Criteria for schools:

  • Located within the Stockholm Region
  • To have one or more SEUs for preschool class, primary school, or middle school students

Inclusion Criteria for students:

  • To be enrolled in a SEU in preschool class, primary school, or middle school
  • To have a documented formal community diagnosis of autism according to ICD-10, or DSM-5 or having related challenges with social communication and interaction as assessed by school staff and guardians.

Exclusion Criteria:

- No exclusion criteria not already mentioned.

Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

DSM diagnostic criteria

The American Psychiatric Association’s manual of mental health diagnoses. DSM-5 (2013, revised as DSM-5-TR in 2022) replaced DSM-IV, and some studies still name the older edition. “Meets DSM criteria for …” means diagnosed by that edition’s diagnostic criteria, usually by a clinician in an interview.

05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
200 participants (estimated)

Study arms

  • Experimental
    Experimental group

    In the experimental group, labeled APERS+, APERS assessments will be carried out to rate the overall program quality for students with autism/SCCs within the SEUs. These ratings will be made by researchers (PI and doctoral candidate) and a team of specially trained coaches consisting of 5-6 special educators working for the educational administration unit (Utbildningsförvaltningen) of Stockholm Municipality. The SEUs will be provided written and oral feedback based on the ratings In the APERS+ contingency, the coaches then develop an action plan in order to improve program quality of the SEUs. Staff in the participating SEUs will also participate in a half-day of lectures and workshops about autism and other SCCs. Coaches will lastly provide weekly or bi-weekly coaching sessions in the SEUs based on the action plan to promote program quality and implement evidence-based practices. The intervention for each SEU will last for approximately 7-8 months.

    Behavioral: APERS+

  • No intervention
    Control group

    In the control group, APERS assessments will also be carried out by researchers and/or coaches. Written and oral feedback will be provided, but no further coaching will be given and no action plan will be created.

Interventions

  • BehavioralAPERS+

    APERS assessments with written and oral feedback. Creation of an action plan that is continuously followed up by specially trained coaches weekly or bi-weekly in coaching sessions designed to support the use of evidence-based practices in school settings. Half-day lecture about autism and related SCCs.

06

What researchers measure

Primary outcomes

  1. Change from baseline in autism program quality as assessed with the Swedish Autism Program Environment Rating Scale - Primary school (APERS-Primary-SE)

    The APERS-Primary-SE is a rating scale designed to examine primary school program quality for students with autism or related sociocommunicative challenges in Sweden. It contains 10 domains including areas such as students' personal independence and competence, and challenging behaviors. The scale consists of 58 items rated on a five-point Likert scale (1= low quality, 5 = high quality) resulting in individual item scores, subdomain scores, domain scores, and a total score.

    Time frame: Baseline and about 8 months from baseline

Secondary outcomes

  1. Change from baseline in how students feel about their school as assessed with How I Feel About My School (HIFAMS)

    The HIFAMS is a questionnaire designed to assess the happiness and subjective well-being of children in school. It will be completed by all participating children in the study. The questionnaire consists of 8 items where the child is asked how they feel about their school life. The items are scored using a three-point facial Likert scale (sad face, neutral face, happy face). The faces are converted into numerical scores (0-2).

    Time frame: Baseline and about 8 months from baseline

  2. Change from baseline in parent ratings on their child's bodily functions, activities, and participation and contextual factors as assessed with the International Classification of Functioning, Disability and Health (ICF) Core Sets for Autism

    The ICF Core Sets for Autism is a questionnaire where parents rate their child's functioning. It contains 37 items pertaining bodily functions, activities and participation as well as contextual factors that may affect the child's functioning. Responses are given on a Likert scale ranging from either 0 to 10 (individual factors) or -5 to 5 (contextual factors), where higher ratings indicate higher levels of functioning and/or participation.

    Time frame: At baseline and 8 months follow-up.

  3. Change in teachers' perceived self-efficacy in supporting students with autism using the Autism Self-Efficacy Scale for Teachers (ASSET)

    The Autism Self-Efficacy Scale for Teachers is a questionnaire where teachers rate their perceived self-efficacy in supporting students with autism and related SCCs in their classroom. It consists of 28 items and is rated on a six-point Likert scale from 0 to 5. Higher ratings indicate higher self-efficacy.

    Time frame: At baseline and 8 months follow-up.

  4. Individual goal attainment as assessed with a Goal Attainment Scale (GAS)

    The Goal Attainment Scale is a scale used to support, monitor and assess individual goal attainment in children with autism. Goals are created collaboratively by teachers and coaches at baseline and tailored to each child's individual needs and capacity. Goal attainment is assessed by coaches at follow-up on a five-step Likert scale, where 0 is baseline and 4 is exceeding goals.

    Time frame: At baseline and 8 months follow-up

Other outcomes

  1. Social validity as assessed with the Social Validity Scale

    A scale designed to asses the social validity of the procedures, goals, and outcomes of the study by participating school staff and coaches. It consists of 12 items rated on a Likert scale from 0 to 5, where higher ratings indicate higher levels of perceived social validity.

    Time frame: Rated at follow-up approximately 8 months after study start

  2. Social responsiveness as assessed with the Social Responsiveness Scale 2 (SRS-2)

    The SRS-2 is a scale designed to identify the presence and severity of social impairment within the autism spectrum and to differentiate it from difficulties associated with other conditions. Used in the current study to assess the level of social challenges for the participating children. The scale contains 65 items and is rated by the children's parents or guardians. Each item is rated on a 4-point Likert scale ranging from 1 to 4, where 1 is "not true" and 4 is "almost always true". Higher scores indicate more severe social impairment associated with autism.

    Time frame: Baseline assessment

07

Study locations

1 site
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 21, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07830160
Lead sponsor
Stockholm University
Responsible party
Hampus Bejno (Associate professor, Stockholm University) — Principal investigator
First posted
Sep 21, 2026
Start date
Sep 20, 2026 (estimated)
Primary completion
Jun 15, 2028 (estimated)
Completion
Jun 15, 2028 (estimated)
Last update
Sep 21, 2026

Study contacts

Hampus Bejnö, PhD
Contact
hampus.bejno@specped.su.se
+46(0)8-12076264

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Aug 2026. You cannot join it, but the record below documents what was studied.

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