ISRCTN11627644
Active, not recruiting
未知
Development, feasibility testing and pilot trial of a crisis planning and monitoring intervention to reduce compulsory hospital readmissions (the FINCH study)
niversity College London0 sites80 target enrollmentMay 25, 2022
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Mental health
- Sponsor
- niversity College London
- Enrollment
- 80
- Status
- Active, not recruiting
- Last Updated
- 2 years ago
Overview
Brief Summary
2024 Protocol article in https://doi.org/10.1186/s40814-024-01453-z (added 22/02/2024)
Investigators
Eligibility Criteria
Inclusion Criteria
- •Service user participants:
- •Eligible participants will:
- •1\. Have been compulsorily detained under section of the Mental Health Act (section 2 or 3\) during their current hospital admission
- •2\. Be due to receive community mental health care locally post\-discharge
- •3\. Be aged 18\+ years
- •4\. Have the capacity to consent at the time of recruitment
- •Clinician participants (for intervention development and evaluation):
- •Eligible participants will be
- •1\. Currently working in an NHS mental health service as a nurse, psychiatrist, psychologist, social worker, occupational therapist, support worker or assistant psychologist
- •2\. Currently working with service users who are currently or recently (in the last year) detained under section of the Mental Health Act (section 2 or 3\)
Exclusion Criteria
- •Service user participants:
- •Participants will be excluded if they:
- •1\. Are already receiving an intensive psychosocial intervention that focuses on crisis reduction (for example, assertive outreach services)
- •2\. Have a diagnosis of dementia or a brain injury
- •3\. Do not speak sufficient English to take part without an interpreter
- •4\. Lack capacity to consent
- •Staff participants and personal mental health workers:
- •Does not meet the inclusion criteria
Outcomes
Primary Outcomes
Not specified
Similar Trials
Completed
Not Applicable
A clinical trial to find out the optimal oral iron dosing schedule for the prevention of anaemia in pregnant women (PANDA-Dose study)Iron supplementation in pregnant womenPregnancy and ChildbirthISRCTN12911644HS Blood and Transplant300
Active, not recruiting
Not Applicable
What are the best ways to improve shared decision-making for all patients booked for surgery?ISRCTN17951423niversity of Bristol130
Active, not recruiting
Not Applicable
Timing an intervention for aortic stenosis with remote patient monitoringRemote monitoring of patients with aortic stenosisCirculatory SystemISRCTN19413194niversity of Birmingham66
Completed
Not Applicable
Impact of a family-centered discharge and follow up programme on survival, growth, and development of high-risk newborns discharged from a neonatal unit in Kiwoko, Central UgandaHigh-risk newbornsNeonatal DiseasesISRCTN51636372Adara Development191
Completed
Not Applicable
Evaluating mobility and strength training with and without protein supplements in pre-frail/frail older adults with low protein intakePre-frail/frail older adults with low protein intakeNot ApplicableISRCTN30405954niversity of Oxford50