Parenting experience borderline personality disorder traits: parent and practitioner perspectives 2018-2019

DOI

This study collected qualitative data to further understanding of parenting experience and support required by this group. This includes data collected from practitioners to incorporate their experiences in working with these parents. Data collection was structured around three research questions: (1) how do individuals with challenges around emotional intensity experience being a parent; (2) what support have they sought and experienced and how effective and appropriate has it been; and (3) what support would they like to receive/have liked to have received? Borderline Personality Disorder (BPD) is characterised by struggles in emotional intensity, changeable moods, challenges in interpersonal relationships, and an increased likelihood of self-harm. When coupled with the challenges of parenting, these characteristics can make it difficult for an individual with BPD to provide stable, responsive and nurturing care to their children and places their children at risk of a range of negative psychological and social outcomes (Petfield, 2015). Unsurprisingly the experience of parenting can be a highly stressful and unsatisfying one (Newman, Stevenson, Bergman, & Boyce, 2007) and can worsen a vulnerable parent’s mental health (Van de Ende, 2016; Berg-nielsen, Vikan, & Dahl, 2002). Although the parenting deficits of individuals struggling with EICM have been identified, there is limited evidence as to the strengths, weaknesses, needs and hopes as described by the parents themselves. This project will utilise a qualitative design to examine the parenting experience of these individuals and the support offered in this domain. A series of semi-structured focus groups will be carried out with parents and practitioners working with parents struggling with EICM. Data will be subject to thematic analysis as part of which parent participants will be invited to engage with the development of themes.

Interviews and focus groups with parents and practitioners at community locations. Ten parents were interviewed alone and two were interviewed as a pair. Interviews were conducted in the home (n = 4), or on NHS sites. All were conducted by the CI, recorded on encrypted Dictaphone and transcribed. 18 practitioners (6 occupational therapists; two family coaches; three clinical psychologists: three nursing professionals; five social workers; one midwife and one charity worker) took part in focus groups -three multi-disciplinary and three were team-based. Three practitioners were interviewed alone. Focus groups and interviews (except one) at NHS sites.

Identifier
DOI https://doi.org/10.5255/UKDA-SN-854245
Metadata Access https://datacatalogue.cessda.eu/oai-pmh/v0/oai?verb=GetRecord&metadataPrefix=oai_ddi25&identifier=a8119ec71a798a5c7cb8018a30e4622cbb3b9cd1c06ebb45c0ae4f0adc21d8d7
Provenance
Creator Dunn, A, University of Sussex
Publisher UK Data Service
Publication Year 2020
Funding Reference Economic and Social Research Council
Rights Abigail Dunn, University of Sussex; The Data Collection is available for download to users registered with the UK Data Service.
OpenAccess true
Representation
Language English
Resource Type Text
Discipline Psychology; Social and Behavioural Sciences
Spatial Coverage Sussex; United Kingdom