The effects of a colorectal cancer screening programme for average-risk older Chinese adults

ISRCTN ISRCTN39658070
DOI https://doi.org/10.1186/ISRCTN39658070
Secondary identifying numbers 21.0205
Submission date
04/08/2022
Registration date
09/08/2022
Last edited
05/12/2023
Recruitment status
No longer recruiting
Overall study status
Completed
Condition category
Cancer
Prospectively registered
Protocol
Statistical analysis plan
Results
Individual participant data

Plain English summary of protocol

Background and study aims
Colorectal cancer screening can help early detection of cancer. Motivational interviewing could be a strategy to increase people's intention and action toward screening. This study aims to estimate the feasibility and acceptability of the intervention and the preliminary estimation of its effect on screening intention and uptake, knowledge and health beliefs of participants.

Who can participate?
People aged between 50-75 years old without a history of colorectal cancer

What does the study involve?
The intervention group receive a motivational interviewing session

What are the possible benefits and risks of participating?
The potential benefits are that the participants may be motivated and have higher self-efficacy to obtain colorectal cancer screening. There are no risks involved in participation.

Where is the study run from?
The Neighbourhood Advice-Action Council (NAAC) (Hong Kong)

When is the study starting and how long is it expected to run for?
November 2021 to March 2022

Who is funding the study?
Investigator-initiated and funded (Hong Kong)

Who is the main contact?
Dr Dorothy Chan (Hong Kong)
dorothycns@cuhk.edu.hk

Contact information

Dr Dorothy Chan
Principal Investigator

ELB 812, 8/F
Hong Kong (China)
852
Hong Kong

Phone +852 39438165
Email dorothycns@cuhk.edu.hk

Study information

Study designExploratory pilot randomized controlled study
Primary study designInterventional
Secondary study designRandomised controlled trial
Study setting(s)Community
Study typeScreening
Participant information sheet Not available in web format, please use the contact details to request a participant information sheet
Scientific titleEffects of a motivation-based, technology-enhanced colorectal cancer screening programme for average-risk older Chinese adults: An exploratory study
Study objectivesParticipants who receive motivational interview sessions and information about access to screening will have colorectal cancer screening uptake
Ethics approval(s)Approved 27/10/2021, The Chinese University of Hong Kong Survey and Behavioral Research Ethics Committee (G/F, Basic Medical Science Building; telephone not available; email not available), ref: SBRE-21-0205
Health condition(s) or problem(s) studiedPrevention of colorectal cancer
InterventionBlock randomisation with varying block sizes (6, 8,10 and 12) was used to optimise allocation concealment and maintain a good balance between groups throughout the subject recruitment period when eligible participants were randomly allocated into either the intervention group or the control group. The assignments to the intervention or control groups were sealed in opaque envelopes. The sequentially numbered, opaque, sealed envelopes were given to the participants in the sequence in which they enter the study.

The intervention group participants receive two sessions of motivational interviewing during the first 2 weeks (once per week, 1 h each), either onsite or through a real-time online Zoom meeting. One week after completing the motivational interviewing sessions, the interventionist will send interactive messages or phone calls to review the screening status of the participants. Participants will be encouraged to undergo screening and be provided with appropriate logistical support regarding the screening workflow (e.g., registration for the electronic health record sharing system, navigating and scheduling appointments). The control group participants receive the usual care and a fact sheet about CRC prevention.
Intervention typeBehavioural
Primary outcome measureFaecal occult blood testing (FOBT)-based colorectal cancer screening uptake measured by checking the original receipt of attendance at 3 months since recruitment
Secondary outcome measures1. Perceived barriers to screening measured using a questionnaire and after completion of the intervention
2. Perceived benefits of screening measured using a questionnaire and after completion of the intervention
3. Perceived self-efficacy of screening measured using a questionnaire and after completion of the intervention
4. Screening intention measured using a questionnaire and after completion of the intervention
5. Knowledge of colorectal cancer and screening measured using a questionnaire and after completion of the intervention
Overall study start date01/11/2021
Completion date31/03/2022

Eligibility

Participant type(s)Healthy volunteer
Age groupAdult
SexBoth
Target number of participants40
Total final enrolment40
Key inclusion criteria1. Age between 50 and 75 years old
2. No history of colorectal cancer and did not have a faecal immunochemical test (FIT) in the past 2 years or colonoscopy in the past 10 years
Key exclusion criteriaDoes not meet inclusion criteria
Date of first enrolment01/11/2021
Date of final enrolment31/03/2022

Locations

Countries of recruitment

  • Hong Kong

Study participating centre

The Neighbourhood Advice-Action Council (NAAC)
Unit 4
Level 3
Community Recreation Building
Shan King Estate
Tuen Mun
852
Hong Kong

Sponsor information

Chinese University of Hong Kong
University/education

Central Avenue
Shatin
None available
Hong Kong

Phone ++852 39437000
Email dorothycns@cuhk.edu.hk
Website http://www.cuhk.edu.hk/english/index.html
ROR logo "ROR" https://ror.org/00t33hh48

Funders

Funder type

Other

Investigator-initiated and funded

No information available

Results and Publications

Intention to publish date31/12/2022
Individual participant data (IPD) Intention to shareNo
IPD sharing plan summaryNot expected to be made available
Publication and dissemination plan1. Planned publication in a high-impact peer-reviewed journal
2. The results will be disseminated at conferences
IPD sharing planThe datasets generated during and/or analysed during the current study are not expected to be made available without consent from participants

Study outputs

Output type Details Date created Date added Peer reviewed? Patient-facing?
Results article 12/10/2023 05/12/2023 Yes No

Editorial Notes

05/12/2023: Publication reference added.
08/08/2022: Trial's existence confirmed by The Chinese University of Hong Kong Survey and Behavioral Research Ethics Committee.