Autistic Eye Contact?
2 other identifiers
observational
30
1 country
1
Brief Summary
This research explored both breadth and depth of the experiences with eye contact in adults with and without ASD. A hermeneutic phenomenological multicenter design was used in which 15 adults with ASD and 15 adults without ASD were interviewed, using semi-structured interviews. Analyses using Multisite Qualitative Analysis (MSQA) and PRICE-model for saturation.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for all trials
Started Jun 2024
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
June 3, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 30, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
September 30, 2024
CompletedFirst Submitted
Initial submission to the registry
March 28, 2025
CompletedFirst Posted
Study publicly available on registry
April 10, 2025
CompletedApril 10, 2025
March 1, 2025
4 months
March 28, 2025
April 3, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Experiences with eye contact with use of semi-structured interviews
The subjective eye contact experiences of adults with ASD compared to adults without ASD, using semi-structured interviews
June to September 2024
Study Arms (2)
Autism
The group of adults with ASD consisted of participants who were receiving outpatient treatment at one of three specialized centers for ASD, located in Deventer, Rotterdam or Amsterdam in the Netherlands.
Neurotypicals
The group of adults without ASD consisted of participants who were never diagnosed with autism and lived in the Netherlands.
Eligibility Criteria
The Netherlands
You may qualify if:
- Diagnosed with autism according to an internationally recognized classification system
- Receiving outpatient treatment at a specialized autism center in the Netherlands
- Being able to understand the themes to be discussed
- Motivation to participate in the research
You may not qualify if:
- Insufficient command of the Dutch language
- Use of alcohol and/or recreational drugs during the study
- Too much mental instability to participate in the study
- Familiarity with treatment in intellectual disability care
- Adults without autism
- Being able to understand the themes to be discussed
- Motivation to participate in the research
- Insufficient command of the Dutch language
- Use of alcohol and/or recreational drugs during the study
- Too much mental instability to participate in the study
- Familiarity with treatment in intellectual disability care
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- UMC Utrechtlead
- Dimence Groepcollaborator
Study Sites (1)
Dimence Groep
Deventer, Overijssel, 7416 SB, Netherlands
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY CHAIR
Nynke Boonstra, Professor
UMC Utrecht
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- CROSS SECTIONAL
- Target Duration
- 1 Year
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- MSc
Study Record Dates
First Submitted
March 28, 2025
First Posted
April 10, 2025
Study Start
June 3, 2024
Primary Completion
September 30, 2024
Study Completion
September 30, 2024
Last Updated
April 10, 2025
Record last verified: 2025-03
Data Sharing
- IPD Sharing
- Will not share
On request.