ISRCTN14710507已完成未知
Female Genital Mutilation: A qualitative study exploring the views of survivors, male partners and healthcare professionals on the timing of deinfibulation surgery (the FGM Sister Study)
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 入组人数
- 141
研究概览
简要总结
2019 Protocol article in https://www.ncbi.nlm.nih.gov/pubmed/31628134 protocol (added 21/10/2019) 2023 Results article in https://doi.org/10.3310/jhwe4771 (added 23/03/2023) 2022 Results article in https://pubmed.ncbi.nlm.nih.gov/36572653/ primary outcome measure (added 23/03/2023)
研究设计
- 研究类型
- Other
入排标准
- 性别
- All
入选标准
- •Work packages 1a and 2a:
- •2. Aged 18 years or older
- •3. UK resident
- •4. Fluent in English, Somali, Arabic and/or French
- •5. Experienced female genital mutilation/cutting (FGM/C)
- •6. Willing and able to provide written informed consent.
- •Work package 1b:
- •2. Aged 18 years or older
- •3. UK resident
- •4. Fluent in English, Somali, Arabic and/or French
- •5. Partner/wife or family member who has experienced FGM/C
- •6. Willing and able to provide written informed consent.
- •Work package 1c:
- •1. Aged 18 years or older
- •2. Fluent in English
- •3. Healthcare professional, including but not limited to:
- •3.1. General practitioners
- •3.2. Practice nurses
- •3.3. Midwives
- •3.4. Obstetrics and gynaecology clinicians
- •3.5. Genitourinary clinicians
- •3.6. Sexual health specialists
- •4. Currently or recently involved (within the last 5 years) in the delivery of care to FGM/C survivors and their families in the UK
- •5. Willing and able to provide written informed consent
- •Work package 2b:
- •1. Aged 18 years or older
- •2. Fluent in English
- •3. Key FGM/C stakeholder, including but not limited to:
- •3.1. Healthcare professionals (see list for work package 1c)
- •3.2. Policy makers
- •3.3. FGM/C specialist researchers/academics
- •3.4. Health economists
- •3.5. Commissioners
- •3.6. Representatives from third sector organisations (e.g. charities and advocacy groups)
- •4. Currently or recently involved (within the last 5 years) in the delivery of care to FGM/C survivors and their families in the UK
- •5. Willing and able to provide written informed consent
排除标准
- •Work packages 1a and 2a:
- •1. Psychological distress related to FGM/C, which prevents them from consenting and/or participating
- •Work package 1b:
- •1. Partner/wife does not consent to their participation (if identified via a WP1a participant)
- •2. Psychological distress related to FGM/C, which prevents them from consenting and/or participating
- •Work packages 1c and 2b have no exclusion criteria.
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