Perinatal severe mental illness Mental and Behavioural Disorders
Conditions
Interventions
WP2: Exploring patient priorities for postpartum SMI treatment and outcomes
Sample size: 60 mothers with experience of postpartum SMI
Recruitment: via NHS Trusts and community organisations
Procedure:
Sponsors
University of Oxford
Eligibility
Sex/Gender
All
Age
18 Years to 100 Years
Inclusion criteria
Inclusion criteria: 1. Aged 18 years or older 2. Able to communicate sufficiently in English or via approved interpretation support to participate meaningfully 3. Willing to take part in the relevant study activities for the work package 4. Have lived experience of receiving care for perinatal severe mental illness (SMI) within the preceding 5 years (from 12 weeks pregnant to up to a year after pregnancy) 5. Willing and able to participate in photovoice workshops (online or in person), including taking or selecting photographs and engaging in group discussion
Exclusion criteria
Exclusion criteria: 1. Individuals who do not have the capacity to provide informed consent
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Lived experiences, barriers, facilitators, vulnerabilities, and opportunities for improving care for people with postpartum severe mental illness (PP-SMI), measured using thematic analysis of three photovoice workshops over 3 weeks at the four study sites (Oxford, London, Sheffield and Lancashire);WP3: positive and negative experiences of the resources from WP1&2, measured using priority setting meetings of 4–6 people at the four study sites;Development of a culturally safe co-designed postpartum severe mental illness care pathway and implementation plan, measured using two in-person half-day co-design workshops over 2 months at each of the four study sites | — |
Secondary
| Measure | Time frame |
|---|---|
| There are no secondary outcomes | — |
Countries
England, United Kingdom
Contacts
Public ContactHarsimran;Roisin Sansoy;Mooney
;
Outcome results
None listed