Ethnicity Data in HIV Positive Men Who Have Sex With Men
Recruitment status was Not yet recruiting
|Study Design:||Observational Model: Cohort
Time Perspective: Retrospective
|Official Title:||Accuracy of Ethnicity Recording in MSM Patients With HIV of Non-White Ethnicity in London|
- Proportion of misclassification of ethnicity for non-White MSM with HIV living in London [ Time Frame: end of study (2 months) ] [ Designated as safety issue: No ]
- • Prevalence of individual non-White self-identified ethnicity groups in MSM with HIV in London [ Time Frame: End of study (2 months) ] [ Designated as safety issue: No ]
- Description of current clinic practice for ethnicity data recording [ Time Frame: End of study (2 months) ] [ Designated as safety issue: No ]
|Study Start Date:||June 2011|
|Estimated Study Completion Date:||July 2011|
|Estimated Primary Completion Date:||July 2011 (Final data collection date for primary outcome measure)|
|Non white HIV positive men who have sex with men|
HIV Doctors will be identified at each of the London HIV treatment centres and details of the project will be communicated to them via email.
These doctors will then be sent paper copies of the patient information sheets (PIS), patient questionnaires and clinician questionnaires.
Eligible patients (i.e. men having sex with men with HIV from non-white ethnic groups) will be identified by their doctors and will be asked to read the PIS and complete the questionnaire. This will be a single questionnaire and no follow up for the patient will be required. No personal information (e.g. date of birth, hospital number) will be recorded. Eligible patients will be all those coming to clinic for HIV care between 1st June and 31st of July 2011. Based on estimates from 2009 data held by the HPA, each doctor will on average be asked to recruit 30 patients over the two month period.
The questionnaire will ask questions regarding self description of ethnicity, sexuality, parents' ethnicity, country of birth and other countries of residency (if relevant). It is anticipated that to read the PIS and complete the questionnaire should take no longer than 15 minutes.
The doctor will then return the paper questionnaire (in an addressed envelope supplied) to Dr Williams. Dr Williams will then bring together and analyse the data from the questionnaires and write up her findings for publication and presentation at a national conference.
Please refer to this study by its ClinicalTrials.gov identifier: NCT01277458
|Contact: Helen Williams, MBBSfirstname.lastname@example.org|
|Guy's and St Thomas' NHS Foundation Trust||Not yet recruiting|
|London, United Kingdom, SE1 7EH|