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Clinical Trials/ISRCTN30846825
ISRCTN30846825
Active, not recruiting
未知

Multi-disciplinary Evaluation of Sexual Assault Referral Centres for better Health (MESARCH)

Coventry University0 sites337 target enrollmentAugust 30, 2019

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
Coventry University
Enrollment
337
Status
Active, not recruiting
Last Updated
3 years ago

Overview

Brief Summary

2022 Protocol article in https://pubmed.ncbi.nlm.nih.gov/35613767/ (added 27/05/2022)

Registry
who.int
Start Date
August 30, 2019
End Date
November 30, 2022
Last Updated
3 years ago
Study Type
Observational
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Current participant inclusion criteria as of 18/09/2020:
  • 1\. Individuals aged \=18 years who have accessed services at a SARC
  • 2\. A small, non\-representative sample of children (aged 13\-15 years) who have accessed services at two paediatric SARCs
  • Previous participant inclusion criteria:
  • 1\. Individuals aged \=16 years who have accessed services at a SARC
  • 2\. A small, non\-representative sample of children (13\-15 years) who have accessed services at one paediatric SARC

Exclusion Criteria

  • Current participant exclusion criteria as of 18/09/2020:
  • 1\. Whilst every effort will be made to ensure inclusivity, service users may be excluded if in exercising judgement the responsible member of SARC staff anticipates that the service user would likely encounter difficulties in providing informed consent or responding to or understanding the content of surveys or interviews used in data collection due to significant mental health issues (psychosis or high risk of suicide), cognitive impairment, or learning disability
  • 2\. People who view information on the SARC website only
  • Previous participant inclusion criteria:
  • 1\. Whilst every effort will be made to ensure inclusivity, service users may be excluded if in exercising judgement the responsible member of SARC staff anticipates that the potential participant would likely encounter difficulties in providing informed consent or responding to or understanding the content of surveys or interviews used in data collection due to significant mental health issues (psychosis or high risk of suicide), cognitive impairment, or intellectual disability
  • 2\. People who access information or support from the SARC by telephone or email only
  • 3\. People who view information on the SARC website only

Outcomes

Primary Outcomes

Not specified

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