Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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NOT_YET_RECRUITING
NA
8 participants
INTERVENTIONAL
2024-03-31
2025-03-31
Brief Summary
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Detailed Description
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There is good evidence to suggest that psychological support at the time of traumatic events reduces the long term psychological consequences ie post traumatic stress disorder. Although national guidelines on PPROM suggest psychological support should be available this is not routine clinical practice and no guidance is given on what form of support this should be.
This pilot study aims to develop a talking therapy based on Cognitive Behavioural Therapy principles to support women and garner their feedback.
A series of 5-8 women who are hospitalised in St Thomas' hospital where their waters have broken before 37 weeks into their pregnancy will be approached by a member of the team of doctors/midwives who are looking after them.
Women will be offered an initial session of assessment by a psychologist to gain an individualised understanding of their current anxiety and mood levels and to assess what is causing stress. This may be thoughts, feelings and behaviours relative to their current mood and aspects of the current situation. A set of strategies will be developed such as education about anxiety and responses to traumatic and upsetting situations, modification of negative thoughts, support with excessive reassurance seeking, self-compassionate exercises to help with self-criticism and self-blame, support with decision-making and strategies to manage uncertainty.
Up to 5 further hour long follow up sessions will occur with the time between sessions and number determined by the woman and her circumstances. Due to the levels of uncertainty associated with the situation, each session will be considered as a stand-alone.
Information about their details (such as age, ethnicity, whether they currently have a partner, details of medical conditions, current and previous pregnancies) will be obtained from participants. A brief measure of mood will be collected at each contact and at 4-6 weeks after the final session. The Hospital Anxiety and Depression scale a validated tool will be used to assess mood.
Given that women will be in the midst of a potentially fast-moving medical context may affect scores to some extent, further feedback will be sought from women at the end of each therapy session and beginning of each subsequent session on how useful they have found the session and interventions suggested.
Detailed notes will be kept on the specific techniques employed in each session and suggested as between session practice.
Conditions
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Study Design
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NA
SINGLE_GROUP
SUPPORTIVE_CARE
NONE
Study Groups
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Psychological intervention
Women will be given psychological intervention
Psychological intervention along Cognitive Behavioural Therapy principles
Women who have PPROM will be offered a series of 6 sessions with a Clinical Psychologist
Interventions
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Psychological intervention along Cognitive Behavioural Therapy principles
Women who have PPROM will be offered a series of 6 sessions with a Clinical Psychologist
Eligibility Criteria
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Inclusion Criteria
* Is experiencing PPROM
* Has been admitted to the ward
* Has capacity to give informed consent to take part in the research
* Speaks and writes English
Exclusion Criteria
16 Years
FEMALE
Yes
Sponsors
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King's College London
OTHER
Responsible Party
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Locations
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St Thomas' Hospital, King's College London
London, Greater London, United Kingdom
Countries
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Other Identifiers
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334235
Identifier Type: -
Identifier Source: org_study_id
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