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Psychoeducation for Adults With Autism and Their Significant Others/Family Members (Prisma)

Karolinska Institute logo

Karolinska Institute

Status

Completed

Conditions

Acceptance of Diagnosis
Stigma of Mental Illness
Quality of Life
Relation, Family
Participation
Depression
Anxiety
Knowledge Acquisition Disability Nos
Treatment Satisfaction

Treatments

Behavioral: Treatment as usual/standard care
Behavioral: Psychoeducation for Adults With Autism and Their Significant Others/Family members (Prisma)

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

Prisma is a four-session psychoeducational intervention administered in groups for individuals with ASD together with their family members and significant others. The aspiration is to make Prisma into an affordable, accessible and available intervention. This includes taking into account a great age spectrum, differences in comorbidity as well as other varied qualities that characterize this group. Acknowledging this diversity and helping to create opportunity for these individuals is of great importance in order to follow national as well as international legislations of the patient's rights.

The aim of the proposed studies is to evaluate the feasibility and effect of Prisma in adults (18 or over) with ASD and their family members/significant others in an outpatient clinical habilitation context.

Full description

Against the background that interest organizations has identified a need for more knowledge about ASD both in adults with ASD and their significant others, a psychoeducational intervention Prisma was created.

Prisma - the psychoeducational intervention The intervention consists of four 2-hour sessions (2 x 45 min lecture plus paus and time for questions). Two clinicians administer each course and follow a power point with detailed instructions. The goal is to increase knowledge and provide the participants with new insights into their diagnosis and that they get concrete tools that will help them handle obstacles in their everyday life. Another important aspect is to learn more about available support and services.

This research project consists of three studies: An open feasibility study , a randomized controlled trail (RCT) including a three month follow-up, a moderation and mediation study including new outcome variables for stigma and participation.

Study 1. The data collection for the open feasibility study was carried out during the fall of 2017. Data remains to be analyzed. n = 186

Study 2. The RCT will include approximately n=80 in the experimental group and equally many wait-list controls. The RCT also include one significant other per patient which gives a total number of 320 in the RCT. Participants are randomized to be in either the experimental group or the wait-list/treatment as usual controls. The experimental groups receive Prisma according to the manual while the wait-list/TAU controls take part in Prisma approximately 4 months later.

Study 3. In order to expand the analyses beyond what is addressed in the RCT (study 2), researchers would like to investigate if increased knowledge of ASD via participation in Prisma will affect self-stigma and/or affiliate stigma. Importantly, stigma will be investigated both in adults with ASD (self-stigma) and in their significant others (affiliate stigma). Yet another expansion of this project that researchers will address in study 3 is the experiences of active participation and engagement during the Prisma program, and possible association between engagement and treatment results for the adults with ASD and their significant others.This study will include 150 adults with ASD and 150 significant others.

Enrollment

718 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adults with autism spectrum disorder
  • Should meet DSM-5 criteria for ASD and/or ICD-10 for one of the autism diagnoses under F84.
  • Diagnoses are set within the Swedish healthcare system
  • The significant other should also be an adult (18 years or older) and could be a parent, sibling, partner, friend or what the participant with ASD thought of as a significant other.

Exclusion criteria

  • Intellectual disability.
  • Insufficient command of the Swedish language/ unable to understand the content.
  • Severe psychiatric comorbidity that made participation difficult (e.g. severe depression, severe suicidality, severe anxiety), other circumstances that could make participation hard (e.g. homelessness) and severe difficulties or discomfort participating in groups.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

718 participants in 2 patient groups

Experimental group
Experimental group
Description:
Experiment group that receives the psychoeducation direct after the baseline measurement.
Treatment:
Behavioral: Psychoeducation for Adults With Autism and Their Significant Others/Family members (Prisma)
Control group
Other group
Description:
Standard care / treatment as usual. Comparison group alos receives Prisma psychoeducation after the three-month follow-up time period.
Treatment:
Behavioral: Treatment as usual/standard care

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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