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Increasing Uptake of Bowel Screening (TEMPO)

Primary Purpose

Colorectal Cancer

Status
Active
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Suggested deadline for return of screening test
Planning sheet
Sponsored by
University of Glasgow
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Colorectal Cancer focused on measuring Early Detection of Cancer

Eligibility Criteria

50 Years - 74 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • 50-74 years
  • Registered with a Community Health Index number in Scotland
  • More than 2 years since last bowel screening invitation

Exclusion Criteria:

  • Has self-excluded from Scottish Bowel Screening Programme
  • Not sent a screening kit by the Scottish Bowel Screening Programme

Sites / Locations

  • Scottish Bowel Screening Centre

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm 5

Arm 6

Arm 7

Arm 8

Arm Type

No Intervention

Experimental

Experimental

Experimental

Experimental

Experimental

Experimental

Experimental

Arm Label

Control

1-week deadline, no planning sheet

2-week deadline, no planning sheet

4-week deadline, no planning sheet

No deadline, with planning sheet

1-week deadline, with planning sheet

2-week deadline, with planning sheet

4-week deadline, with planning sheet

Arm Description

Outcomes

Primary Outcome Measures

Number of screening tests returned to the central laboratory and successfully processed providing an adequate result.

Secondary Outcome Measures

Number of screening tests returned to the central laboratory
Number of screening tests returned to the central laboratory within suggested deadline
Number of screening tests returned to the central laboratory by area-level deprivation
Cognitive and behavioural mechanisms
A questionnaire designed to assess mechanisms, e.g. action and coping planning, using items adapted for the bowel screening context.
Acceptability of interventions (quantitative)
The Acceptability Questionnaire
Acceptability of interventions (qualitative)
Analysis of in-depth semi-structured interviews.

Full Information

First Posted
April 29, 2022
Last Updated
August 8, 2022
Sponsor
University of Glasgow
Collaborators
NHS Greater Glasgow and Clyde, NHS Tayside, University of Cambridge, University of St Andrews, University of Stirling, University of Dundee, Chief Scientist Office of the Scottish Government, Cancer Research UK
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1. Study Identification

Unique Protocol Identification Number
NCT05408169
Brief Title
Increasing Uptake of Bowel Screening
Acronym
TEMPO
Official Title
Increasing Uptake of Faecal Immunochemical Test (FIT) Bowel Screening: Trial of Providing a Suggested Deadline for FIT Kit Return and a Planning Sheet
Study Type
Interventional

2. Study Status

Record Verification Date
August 2022
Overall Recruitment Status
Active, not recruiting
Study Start Date
June 20, 2022 (Actual)
Primary Completion Date
October 2022 (Anticipated)
Study Completion Date
January 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Glasgow
Collaborators
NHS Greater Glasgow and Clyde, NHS Tayside, University of Cambridge, University of St Andrews, University of Stirling, University of Dundee, Chief Scientist Office of the Scottish Government, Cancer Research UK

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Bowel cancer is the second biggest cancer killer in the UK, accounting for over 16,000 deaths per year. Screening can reduce deaths from bowel cancer if the people invited participate. The challenge is that high uptake of bowel screening is hard to achieve, and remains persistently below 65%. The faecal immunochemical test (FIT) is the most widely used bowel screening test worldwide. In the UK, FIT kits are mailed to people's homes without guidance on when the kit should be returned and only brief instruction on how to use it. Some people have said that even though they intend to complete and return the kit, they often forget or put off doing it. Two approaches are proposed to addressing this issue: i) providing a suggested deadline for FIT return, because it is known from breast and cervical cancer screening that giving people an appointment time increases uptake compared to an open invitation, and ii) planning sheets, that have been found to help people act on their intentions in other health contexts. This trial aims to evaluate the impact of providing a suggested deadline and a planning sheet on the return of FIT bowel screening kits. The trial is integrated within the Scottish Bowel Screening Programme. The investigators will randomly allocate 40,000 consecutive people that are due to be sent a FIT kit to one of eight groups: (i) control group (no deadline, no planning sheet), (ii) intervention group (1-week deadline, no planning sheet), (iii) intervention group (2-week deadline, no planning sheet), (iv) intervention group (4-week deadline, no planning sheet), (v) intervention group (no deadline, with planning sheet), (vi) intervention group (1-week deadline, with planning sheet), (vii) intervention group (2-week deadline, with planning sheet), (viii) intervention group (4-week deadline, with planning sheet). It will then be examined if having a suggested deadline and a planning sheet affects how many people send back their completed FIT kit. It will also be examined if the deadline length makes a difference and whether having both a deadline and a planning sheet affects the number of people returning their kit. Finally, the cognitive and behavioural mechanisms underlying any intervention effects will be assessed and the acceptability of the interventions explored, using questionnaires and in-depth interviews.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Colorectal Cancer
Keywords
Early Detection of Cancer

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Factorial Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
40000 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Control
Arm Type
No Intervention
Arm Title
1-week deadline, no planning sheet
Arm Type
Experimental
Arm Title
2-week deadline, no planning sheet
Arm Type
Experimental
Arm Title
4-week deadline, no planning sheet
Arm Type
Experimental
Arm Title
No deadline, with planning sheet
Arm Type
Experimental
Arm Title
1-week deadline, with planning sheet
Arm Type
Experimental
Arm Title
2-week deadline, with planning sheet
Arm Type
Experimental
Arm Title
4-week deadline, with planning sheet
Arm Type
Experimental
Intervention Type
Behavioral
Intervention Name(s)
Suggested deadline for return of screening test
Intervention Description
A screening invitation letter modified to state, highlighted in yellow: "Please return your kit within [X] weeks (by [DD.MM.YYYY]) or as soon as possible."
Intervention Type
Behavioral
Intervention Name(s)
Planning sheet
Other Intervention Name(s)
Volitional help sheet
Intervention Description
A planning tool presented on a separate single sheet of paper inserted into the screening invitation envelope. The colour illustrated tool prompts participants to identify concerns they have with using the bowel screening kit and to link them to a tip to help them overcome this concern.
Primary Outcome Measure Information:
Title
Number of screening tests returned to the central laboratory and successfully processed providing an adequate result.
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Number of screening tests returned to the central laboratory
Time Frame
3 months
Title
Number of screening tests returned to the central laboratory within suggested deadline
Time Frame
1/2/4 weeks
Title
Number of screening tests returned to the central laboratory by area-level deprivation
Time Frame
3 months
Title
Cognitive and behavioural mechanisms
Description
A questionnaire designed to assess mechanisms, e.g. action and coping planning, using items adapted for the bowel screening context.
Time Frame
3 months
Title
Acceptability of interventions (quantitative)
Description
The Acceptability Questionnaire
Time Frame
3 months
Title
Acceptability of interventions (qualitative)
Description
Analysis of in-depth semi-structured interviews.
Time Frame
3-8 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
50 Years
Maximum Age & Unit of Time
74 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: 50-74 years Registered with a Community Health Index number in Scotland More than 2 years since last bowel screening invitation Exclusion Criteria: Has self-excluded from Scottish Bowel Screening Programme Not sent a screening kit by the Scottish Bowel Screening Programme
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Katie Robb
Organizational Affiliation
University of Glasgow
Official's Role
Principal Investigator
Facility Information:
Facility Name
Scottish Bowel Screening Centre
City
Dundee
Country
United Kingdom

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Outcomes 1-4: Details of the dataset and work arising from it will be available from the Robertson Centre for Biostatistics Analytical Platform at the University of Glasgow. The dataset will be archived on live servers within the facility. Use of anonymised data within research is given for the specified project purpose, future use is permitted but would require permission from LPAC and the Caldicott Guardian. Outcomes 5-6: Quantitative data (SPSS files with metadata) and qualitative data (stored as MSword transcripts with metadata) will be deposited in Enlighten: Research Data, the University of Glasgow's institutional data repository. Data in the repository will be stored in accordance with funder and University data policies. Files will be given a Digital Object Identifier (DOI) and the associated metadata will be listed in the University of Glasgow Research Data Registry and the DataCite metadata store.
IPD Sharing Time Frame
Outcomes 1-4: 5 years post completion and data then moved to off-line storage. Outcomes 5-6: 10 years from date of deposition in the first instance, with extensions applied to datasets which are subsequently accessed.
IPD Sharing Access Criteria
Outcomes 1-4: There is no requirement for a data sharing agreement with the research team and no restrictions on data sharing. Any research group can approach and request permission to use datasets. Outcomes 5-6: Data made public at the time of publication.

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Increasing Uptake of Bowel Screening

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