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An Observational Study of GP Verbal Reminders Upon Cervical Screening (VRCS)

D

Dr. Faizan Awan

Status

Completed

Conditions

Physician-Patient Relations
HPV-Related Cervical Carcinoma

Treatments

Behavioral: Cervical Screening Reminder

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

Cervical cancer screening is offered to all women in the United Kingdom (UK) between the ages of 24.5 and 64 years of age. The majority of screening is performed in primary care and the rate remains stubbornly below 80%, despite an automated national invitation system. This study is designed to assess the effectiveness of a physician invitation during a telephone or face-to-face primary care appointment upon non responders of automated invitations, to increase the uptake of cervical screening.

Full description

It is estimated that between 800 and 2,000 deaths a year are now prevented due to the effectiveness of the UK's national cervical screening programme and mortality rates have dropped by over 75% since the 1970s. These statistics corroborate the importance of the screening programme in reducing mortality from cervical cancer. Cervical screening rates in the UK remains stubbornly below 80% and interventions are needed to attract the 20% who are missing out on screening. This prospective observational study is designed to measure the impact of a physician intervention in a usual healthcare environment, amongst a heterogeneous patient population to yield replicable real-world results. The intervention arm will receive a physician intervention to inform them of their overdue screening status, remind them of the importance of cervical screening and guide them to book a screening appointment. The screening rate in the intervention arm will be compared to a control made up of patients seen by other clinicians and receiving unstructured reminders. The results will assist physicians in deciding whether a structured intervention is anymore effective than the unstructured advice currently given at improving screening rates in the non responder population.

Enrollment

724 patients

Sex

Female

Ages

25 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Registered patient with a cervix
  • Non responder to cervical screening invitation

Exclusion criteria

  • Incorrectly reminded i. Coding errors ii. Human error
  • Temporary patients i. Did not remain registered for minimum of 6 months following intervention
  • Screening refusal
  • Inappropriate to include i. Terminal illness ii. Prolonged hospitalisation iii. Death due to non-cervical cancer attributable cause

Trial design

724 participants in 2 patient groups

Intervention
Description:
The principal investigator reviews the medical notes of all individuals they consult over a period of three years to check if they are non responders. If confirmed as non responder, they receive a three-step verbal intervention: 1. "Your cervical cancer screening is now overdue." 2. "The test is easy to perform and saves thousands of lives from cervical cancer every year." 3. "Should we book an appointment for cervical screening now so that you make sure you have it done?" Those who are seen face-to-face receive a fourth intervention: 4. An appointment slip is given to the patient to hand to the receptionist. This includes the patient's name and the comment, "book an appointment with practice nurse for cervical screening".
Treatment:
Behavioral: Cervical Screening Reminder
Control
Description:
The control group receives standard unstructured reminders regarding their overdue status from any of the 6 other clinicians during appointments and / or reminder letters from the administration team.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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