Using Patient Navigation to Promote Bowel Screening in AAA Attendees.

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexMale
Age65+
SponsorUniversity of Surrey

About this trial

The goal of this single-arm, multi-centre feasibility study is to assess the efficacy, feasibility and acceptability of implementing patient navigation across Abdominal Aortic Aneurysm (AAA) screening services in England to increase uptake of bowel cancer screening. The main questions it aims to answer are:

* Do service users complete a bowel cancer screening within three months of receiving patient navigation? * Do service deliverers consider patient navigation as feasible to implement in practice? * Do service users consider patient navigation acceptable to receive during their AAA appointment? Participants will be asked to discuss bowel screening with AAA practitioners (patient navigation). Follow-up surveys and interviews will be conducted with those that delivered the intervention and with those that received it.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Men aged 65 years and above

Attending an AAA screening appointment

Have not completed their most recent bowel screening

Agree to discuss bowel screening further

Disqualifiers

Men aged <65years

Those who do not attend their AAA screening appointment

Have completed their most recent bowel screening

Do not agree to discuss bowel screening further

Trial design

Design model

Single group

Treatments tested in this trial

  • Patient Navigation conversation

    Other intervention

    Brief 1.5-2 minute conversation to discuss barriers and solutions to why have not completed most recent bowel screening. Offer of third party request or information to contact screening service.

Treatment groups

4,190 Participants
are divided into 1 treatment group
Group A: Patient NavigationOther 1 intervention

Trial outcomes

Primary outcomes

1

Number of FIT test completed

Completion of FIT test

Time frame
Completion within 3 months of patient navigation intervention

Secondary outcomes

1

Feasibility of delivering patient navigation (survey)

Survey with those who delivered patient navigation. Survey contains 7 items: 2 demographic questions, 2 items on a 3-point Likert scale (with option to provide further detail in open text), 2 open text responses, and one dichotomous item (Yes/No). The Likert scales are scored where 1 is low and 3 is high.

Time frame
0-5 months post patient navigation delivery
2

Feasibility of delivering patient navigation (Interviews)

Semi-structured interviews with those who delivered patient navigation

Time frame
0-5 months post patient navigation delivery
3

Acceptability of receiving patient navigation (Survey)

Survey with service users who received patient navigation. Survey contains 12 items: 4 demographic questions, 5 items on a 5-point Likert scale, and 3 open text responses. The Likert scales are scored where 1 is high and 5 is low.

Time frame
0-5 months post patient navigation
4

Acceptability of receiving patient navigation (Interviews)

Semi-structured interviews with service users who received patient navigation

Time frame
0-5 months post patient navigation

Other outcomes

Sponsors and contacts

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University of Surrey

Lead sponsor

Cancer Research UK

Collaborator

NHS England

Collaborator

This trial is not recruiting at the moment. You can still explore other options: