Interviews for "Living with Paediatric Acute-onset Neuropsychiatric Syndrome (PANS) – a Qualitative Study of Children’s Experiences in Sweden"
Citation and access
Citation and access
Data access level:
Creator/Principal investigator(s):
Research principal:
Data contains personal data:
Yes
Type of personal data:
Health data
Sensitive personal data:
Yes
Citation:
Language:
Method and outcome
Method and outcome
Unit of analysis:
Population:
Children with PANS
Time method:
Sampling procedure:
Description of sampling:
The recruitment of children and adolescents diagnosed with PANS was done via advertisement on the websites of patient organizations, and in waiting rooms at child and youth medical clinics. Inclusion criteria for participation were children and youth aged 10 to 18 years, with a formal diagnosis of PANS. Participants varied in terms of the child’s age at the time of the interview as well as at the time of diagnosis, the course of the symptoms (i.e. episodic or chronic-static), the illness severity, treatment experiences, and sociocultural background. Participants also varied in what region of Sweden they lived in, as well as if they lived in rural villages or midsize or large cities. The variation in the regions of residence is relevant in the Swedish context, as every region has its own healthcare system.
Time period(s) investigated:
Number of individuals/objects:
7
Data format/data structure:
Data collection - Interview
Data collection - Interview
Mode of collection:
Interview
Source of the data:
- Communications
Geographic coverage
Geographic coverage
Geographic location:
Administrative information
Administrative information
Responsible department/unit:
Department of Special Education
Ethics Review:
Swedish Ethical Review Authority - 2020-06554
Topic and keywords
Topic and keywords
Standard för svensk indelning av forskningsämnen 2025:
Publications
Publications
Citation:
Metadata
Metadata
