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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04058418
Other study ID # 19049
Secondary ID
Status Completed
Phase
First received
Last updated
Start date July 22, 2019
Est. completion date December 31, 2019

Study information

Verified date March 2023
Source University of Nottingham
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Some women are more likely to get breast cancer as it runs in their family, they are at risk of familial breast cancer. There are medications, called chemoprevention, which may lower their risk of developing breast cancer by a third. However chemoprevention can also cause serious side effects, like womb cancer and blood clots. This makes decision to start them difficult. Researchers found that not all women who can have these medications are on them. The investigators want to ask familial breast cancer specialists whether they recommend general practitioners (GP) to prescribe chemoprevention, by sending them a short survey. These specialists look after women where breast cancer runs in the family. The specialists assess a women's chance of getting breast cancer and advice those with increased risk what can be done to prevent breast cancer. The investigators will then look at whether specialist recommendation makes a difference to whether GPs prescribe chemoprevention medication. This will be done by linking the specialists' survey response to information on GP prescribing that the government regularly publishes. This may help the investigators understand why chemoprevention is not used as often as it potentially can be.


Description:

Phase I: Short survey of lead clinicians of familial cancer services, descriptive analysis of recommendations by areas of the country Phase II: Prescribing data analysis (using OpenPrescribing) comprising: 1. t-test to compare the chemoprevention prescribing rate in general practices where chemoprevention is recommended versus not recommended; 2. interrupted times series analysis to assess the change in the chemoprevention prescribing after recommendation from specialist compared with changes occurring in practices where chemoprevention is not recommended and 3. panel regression across all practices, in order to distinguish the relative impacts of national versus local recommendation, and the change over time.


Recruitment information / eligibility

Status Completed
Enrollment 50
Est. completion date December 31, 2019
Est. primary completion date December 31, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Lead clinicians of NHS familial cancer services across England - Standard general practices (classed as type 4 by NHS Digital, to exclude walk-in centres, prisons, care homes, etc.) with prescribing data for chemoprevention available on OpenPrescribing Exclusion Criteria: - General practices with less than 10 female patients aged 35 to 44 registered - General practices which cannot be linked to any familial cancer service from survey responses

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Survey Administration
Completion of a short survey.

Locations

Country Name City State
United Kingdom University of Nottingham Nottingham

Sponsors (2)

Lead Sponsor Collaborator
University of Nottingham University of Oxford

Country where clinical trial is conducted

United Kingdom, 

References & Publications (2)

Curtis HJ, Walker AJ, Goldacre B. Impact of NICE guidance on tamoxifen prescribing in England 2011-2017: an interrupted time series analysis. Br J Cancer. 2018 May;118(9):1268-1275. doi: 10.1038/s41416-018-0065-2. Epub 2018 Apr 23. — View Citation

Qureshi N, O'Flynn N, Evans G. Dealing with family history of breast cancer: something new, something old. Br J Gen Pract. 2014 Jan;64(618):6-7. doi: 10.3399/bjgp14X676267. No abstract available. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Proportion of specialist service that recommends chemoprevention prescribing by areas in England Proportion of specialist service that recommends chemoprevention prescribing by areas in England, measured using survey questionnaire 2019
Primary Chemoprevention medication prescribing rates in primary care by area in England 2.1. The chemoprevention prescribing rate in general practices where chemoprevention is recommended versus not recommended. The rate will be measured as the number of average daily quantities (ADQs) of chemoprevention prescribed per 1000 registered female patients aged between 35 and 74 per practice. For our primary outcome we will measure only tamoxifen items, and assess other therapies used in chemoprevention in supplementary analyses.
2.2. The change in chemoprevention prescribing rate (described in outcome 2.1) in general practices after recommendation from local specialist, compared with changes occurring in practices where chemoprevention is not recommended.
2.3. The relative change in the chemoprevention prescribing rate (described in outcome 2.1) in general practice in response to local recommendation, compared with change occurring in response to national recommendation.
post specialist recommendation over 24 months
See also
  Status Clinical Trial Phase
Completed NCT00040222 - Clinical, Genetic, Behavioral, Laboratory and Epidemiologic Characterization of Individuals and Families at High Risk of Breast/Ovarian Cancer
Enrolling by invitation NCT04197856 - Direct Information to At-risk Relatives N/A