- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04302753
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
-
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Yorkshire And Humber
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Sheffield, Yorkshire And Humber, United Kingdom, S1 2LT
- DClin Univeristy of Sheffield
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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.
Sponsor
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
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 164845
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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