VR is a feasible instrument in training social cognition, decreasing social anxiety and improving overall social functioning
ID
Bron
Verkorte titel
Aandoening
Autism Spectrum Disorder (ASD)
Ondersteuning
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
We will test the VR Social Cognition Training (SCT)for people with ASD in a feasibility study. We will evaluate the feasibility, acceptability and explore the efficacy of VR SCT, and based on the results, improve the intervention protocol using input from clinical providers (experts by training) and participants (experts by experience).
In a pilot-study we explore a Virtual Reality based intervention, to enhance social cognition of adults diagnosed with autism. Primary outcomes of this study are:
- Feasibility and Acceptance of the intervention
Achtergrond van het onderzoek
Rationale: People with autism spectrum disorder (ASD) commonly experience deficits in social cognition, skills and functioning. Social cognition training (SCT) has been shown to have beneficial effects on social cognition tasks, but generalization to social functioning in daily life is limited. Current individual SCT does not seem to be ecologically valid, and patients cannot practice skills in dynamic social interactions. We propose that this problem could be solved by providing SCT in Virtual Reality (VR). VR allows for practice of skills in situations resembling real life, yet remaining safe and controllable.
Objectives: To 1) determine the feasibility and acceptability of VR SCT on patients and for clinicians, and 2) explore the effects of VR SCT on social cognition, social anxiety, social behaviours and cognitive flexibility (neurocognitive measure) and in people with ASD.
Study design: Pre-post design; this study is a feasibility study in a patient group with an autism spectrum disorder. Patients will receive the training, pre-, post-intervention and follow-up assessments will be obtained.
Study population: 25 individuals with a confirmed clinical diagnosis of autism spectrum disorder and social cognition problems, aged 18-65.
Intervention: The VR SCT consists of sixteen sessions, during an 12-week timeframe. Sessions last 60 minutes. During sessions, social cognition is trained in virtual environments. The intervention consists of three modules: facial affect recognition, emotion recognition within a context &theory of mind and interaction training.
Main study parameters/endpoints:
Primary outcome: Acceptability and feasibility of the training, measured using questionnaires and interviews.
Secondary outcome: social cognitive, social anxiety, social behavioural, neurocognitive outcome measures and social functioning.
Nature and extent of the burden and risks associated with participation, benefit and group relatedness: Participants will be interviewed at screening and tested at baseline, post intervention, and at follow-up, with an average total duration of approximately one hour to 75 minutes for each assessment, and 10 minutes for the screening. The intervention will take sixteen hours in total (sixteen sessions of 60 minutes each). We expect patients to benefit from the therapy by increasing social cognitive skills. Some patients might experience simulator sickness symptoms during the therapy. No major adverse events are expected or have been documented previously with a similar VR-SCT protocol (Pot-Kolder et al., 2018).
Doel van het onderzoek
VR is a feasible instrument in training social cognition, decreasing social anxiety and improving overall social functioning
Onderzoeksopzet
Pre-assessment (T0)
Post-assessment (T1)
Follow-up (T2 - 16 weeks after T1)
Onderzoeksproduct en/of interventie
Protocolized Virtual Reality social cognition training
Publiek
Björn Jaime van Pelt
088-4056979
b.vanpelt@yulius.nl
Wetenschappelijk
Björn Jaime van Pelt
088-4056979
b.vanpelt@yulius.nl
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
In order to be eligible to participate in this study, a subject must meet all of the following criteria:
1. Diagnosis of an autism spectrum disorder, determined by a structured observation (ADOS in the previous three years) or a confirmed ASD diagnosis by a clinician
2. Age 18 – 65
3. Indication of impaired social cognition by the treating therapist,
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
A potential subject who meets any of the following criteria will be excluded from participation in this study:
1. An estimated IQ below 70
2. Substance dependence
3. Insufficient proficiency of the Dutch language
4. Presence of a relevant psychiatric or neurological disorder such as dementia, epilepsy or organic brain damage
Opzet
Deelname
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In overige registers
Register | ID |
---|---|
NTR-new | NL8069 |
Ander register | METC ErasmusMC / NL65384.078.18 : MEC-2018-135 |