Autistic Women's Experiences of Self Compassion and Receiving Their Diagnosis in Adulthood

May 5, 2021 updated by: University of Sheffield
Research highlights strong links between self-compassion and mental health, but there is very limited research specifically exploring autistic individual's experiences of self-compassion. The process of receiving a diagnosis on the autism spectrum can be complex and autistic women tend to experience several barriers to diagnosis. This study adds to the growing area of research exploring autistic women's experiences of receiving a diagnosis in adulthood. This study employs Interpretative phenomenological analysis to explore if receiving a diagnosis of Autism influences women's perceptions of self-compassion. The findings may inform client-centred practices in health care settings and potentially present positive aspects of autism diagnosis.

Study Overview

Status

Completed

Conditions

Study Type

Observational

Enrollment (Actual)

12

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Yorkshire And Humber
      • Sheffield, Yorkshire And Humber, United Kingdom, S1 2LT
        • DClin Univeristy of Sheffield

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 99 years (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

N/A

Genders Eligible for Study

Female

Sampling Method

Non-Probability Sample

Study Population

Women who have received their diagnosis on the autism spectrum over the age of 18 years old.

Description

Inclusion Criteria:

  • Able to consent to participate
  • Cisgender female (female at birth and raised as female).
  • Speak English fluently
  • Received an Autism Spectrum Disorder diagnosis, aged 18 years old or above

Exclusion Criteria:

  • Lack capacity to consent to participate in the study
  • Unable to speak English fluently
  • Have not received an Autism diagnosis
  • Have received Autism diagnosis prior to their 18th birthday
  • Have an intellectual disability
  • Born male

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Experience of receiving ASD diagnosis in adulthood based on semi structured interviews
Time Frame: day one
Participants' experience of receiving ASD diagnosis in adulthood based on semi structured interviews, completed in one interview.
day one

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Experience of self-compassion before and after receiving ASD diagnosis based on semi structured interviews
Time Frame: day one
Participants' experiences of self-compassion before and after receiving ASD diagnosis based on semi structured interviews, completed in one interview.
day one

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (ACTUAL)

August 12, 2019

Primary Completion (ACTUAL)

December 1, 2020

Study Completion (ACTUAL)

March 29, 2021

Study Registration Dates

First Submitted

February 13, 2020

First Submitted That Met QC Criteria

March 6, 2020

First Posted (ACTUAL)

March 10, 2020

Study Record Updates

Last Update Posted (ACTUAL)

May 6, 2021

Last Update Submitted That Met QC Criteria

May 5, 2021

Last Verified

March 1, 2020

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

All electronic data including transcripts and audio recordings will be stored in the university data repository, until publication and dissemination of the study is completed. The paper copies of anonymized interview transcripts will be stored in a locked cabinet in the research administration office at the university of Sheffield, for a maximum of six years and then destroyed confidentially.

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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