Developing an Intervention Facilitating the Use of Eye Contact in Adults With Autism

NCT ID: NCT06924008

Last Updated: 2025-04-11

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Total Enrollment

18 participants

Study Classification

OBSERVATIONAL

Study Start Date

2025-07-07

Study Completion Date

2026-11-02

Brief Summary

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The aim of this study is to develop a methodological intervention for adults with autism that will help them reduce problems arising from eye contact.

Detailed Description

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Eye contact is fundamental to human interaction, not only in terms of the experience of connection with others, but also in terms of cognitive skills and social-emotional development. In adults with autism, eye contact is sometimes atypical, which in individual cases can lead to problems in the aforementioned areas. An intervention could possibly lead to a reduction of these problems. However, to date, there is no insight into the problems that this population experiences due to eye contact, how this differs from people without autism, to what extent adults with autism wish to optimize eye contact with others, what they themselves see as solutions for this, and when it proves fruitful to develop an intervention based on all these facets; what an effective intervention could be for this (and who the target group is). While insight into all of this could lead to a reduction in problems that adults with autism and/or their interaction partner experience due to their eye contact. To gain this insight, it is necessary to inventory, among both adults with and without autism, what problems adults with autism actually experience with regard to eye contact, and what their ideas are to reduce these problems. In addition, it is necessary to investigate in a substantiated methodical way which intervention forms a solution for the distilled problems and to test these, in order to be able to assess their effectiveness. If effective, then this intervention could at least contribute to the well-being of adults with autism and a mutually pleasant contact with interaction partners. The current study aims to provide for this and to arrive at an effective intervention that will help adults with autism experience less difficulty as a result of eye contact.

The research design chosen is qualitative research using triangulation by means of descriptive research in the form of semi-structured interviews and Intervention Mapping. The interviews have now taken place. These interviews, in addition to available scientific literature on eye contact in adults with autism, form the starting point for intervention development by means of Intervention Mapping. Intervention Mapping was chosen because the goal is to develop an intervention that will later be as effective as possible. This can be achieved by carefully weighing and substantiating the choices for the goal and the approach in the design phase. Intervention Mapping provides a theoretical basis for the intervention, which makes it more likely that the intervention will also work in practice. In addition, it provides a systematically described intervention and an implementation plan, making the intervention transferable and easier to put into practice. A major advantage of Intervention Mapping is that attention is paid to the way in which the results and effects of the project should be evaluated later, already in the development phase. In this way, Intervention Mapping contributes to increasing the effectiveness of the project. The aim of Intervention Mapping is to provide a framework for effective decision-making at every step of planning, implementation and evaluation. The Intervention Mapping protocol consists of six steps, with a number of tasks described for each step. Although Intervention Mapping is presented as a series of steps, it can be seen as iterative rather than linear. Programme planners switch back and forth between tasks and steps. The process is also cumulative: each step is based on previous steps.

Conditions

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Autism Spectrum Disorder (ASD) Relative (Related Person) Care Giver

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

CROSS_SECTIONAL

Eligibility Criteria

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Inclusion Criteria

* Adults classified with autism, determined according to an internationally recognized classification system.
* Outpatient treatment within a specialized autism center in the Netherlands.
* Able to understand the topics to be discussed.
* Motivation to participate in research.


* Adults without DSM classification.
* Living in the Netherlands.
* Able to understand the topics to be discussed.
* Motivation to participate in research.


* Practicing psychiatrist, clinical psychologist or nurse specialist at an autism expertise center in the Netherlands.
* Living in the Netherlands.
* Motivation to participate in research.

Exclusion Criteria

* No good command of the Dutch language.
* Use of alcohol and/or recreational drugs during the study.
* Mentally too unstable to participate in the study.
* Familiarity with treatment in the VGZ.


* No good command of the Dutch language.
* Use of alcohol and/or recreational drugs during the study.


\- No good command of the Dutch language.
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Dimence Groep

UNKNOWN

Sponsor Role collaborator

UMC Utrecht

OTHER

Sponsor Role lead

Responsible Party

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Jos Boer

MSc

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Nynke Boonstra, Professor

Role: STUDY_CHAIR

UMC Utrecht

Locations

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Dimence Groep

Deventer, Overijssel, Netherlands

Site Status RECRUITING

Countries

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Netherlands

Central Contacts

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Jos Boer, MSc

Role: CONTACT

+31 6 20083507

Nynke Boonstra, Professor

Role: CONTACT

Facility Contacts

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Nynke Boonstra, Professor

Role: primary

+31 6 22678011

Bram Sizoo, Professor

Role: backup

Other Identifiers

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Dimence Groep

Identifier Type: OTHER

Identifier Source: secondary_id

559903

Identifier Type: -

Identifier Source: org_study_id

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