AzTrials
AzTrials

No ConditionSMSNCT07112729

Effectiveness of SMS Invitation on Colorectal Cancer Screening on 45-49-Year-Olds

A study testing Active SMS Invitation in people with No Condition, run by Chang Gung University at 1 site in Taiwan.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
Search all trials

Trial summary

The goal of this study is to learn if sending text message invitations increases participation in colorectal cancer screening among 45-49 year olds in Yingge District, New Taipei City. It will also assess the effectiveness of this method. Read more about this study

Who is it for?
Ages 45 to 49 yearsHealthy volunteers can take part
Conditions the study is for
No Condition
What is being tested?
Active SMS Invitation
Could I receive a placebo?
No, everyone receives an active treatment
How many people
6,708 participants
Where
1 siteTaiwan
Study dates
7 Aug 2025to 18 Sep 2025
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 45 to 49 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • Residents aged 45-49 in Yingge District, New Taipei Cit
  • Must have registered mobile numbers

Who cannot join

  • Not resident in Yingge District
  • Age not in 45-49
  • Without registered mobile phone numbers

Trial locations and contacts

1 site in 1 country.

Taiwan1 site
  • Yingge District Public Health Center, New Taipei City

    New Taipei City

Other trials in Taiwan

About this study

Official title: A Randomized Controlled Trial Evaluating the Effectiveness of SMS Invitations to Increase Colorectal Cancer FIT Screening Rates Among 45-49-Year-Old Residents

The goal of this study is to learn if sending text message invitations increases participation in colorectal cancer screening among 45-49 year olds in Yingge District, New Taipei City. It will also assess the effectiveness of this method. The main questions it aims to answer are:

•Does sending text message invitations increase the number of residents who complete fecal occult blood test (FOBT)? This study will compare a group receiving text message invitations to a control group receiving standard notifications to see if text messages are an effective way to increase screening rates.

Read more

Participants will:

  • Be randomly assigned to either receive text message invitations or standard notifications.
  • The intervention group will receive an initial text and a reminder text one week later.
  • The control group will receive standard notifications, and after one month will receive the same text message.
  • The study will track who obtains a FOBT kit and who completes the test within a three-month period.
Read the detailed description

This study is a randomized controlled trial designed to evaluate the effectiveness of active SMS (Short Message Service) invitations for increasing participation in colorectal cancer screening among residents aged 45-49 in Yingge District, New Taipei City.

Background: Colorectal cancer is a significant public health concern, and early detection through screening is crucial for improving outcomes. This study aims to explore a simple and cost-effective method to increase screening rates in a specific population group (45-49 years old) where screening just initiated.

Objectives: The primary objective is to assess whether sending active SMS invitations increases the rate of fecal occult blood test (FOBT) completion among the target population.

Study Design: The study employs parallel randomized controlled trial design.

Eligible participants will be randomly assigned to one of two groups:

  • Intervention Group (Active SMS Invitation): Participants in this group will receive a text message inviting them to participate in the free FOBT program. The SMS message will include a brief explanation of the program, instructions on how to obtain a screening kit, and a contact number for inquiries. A reminder SMS message will be sent one week after the initial message.
  • Control Group (Standard Notification): Participants in this group will receive the standard notification procedures typically used to inform residents about the FOBT program. After one month of the first SMS sent to the Intervention Group, the Control group will receive the same SMS message as the intervention group.

Intervention:

The contents of SMS is "大腸癌年輕化!國家新政策,符合45-49歲,歡迎參加公費糞便潛血篩檢,顧健康自己來。即日起至8/31止,週一~五8:30-11:30至本所可領採檢管或諮詢電話:098176819鶯歌衛生所關心您。 In English: "Colorectal cancer is affecting younger people! Under a new national policy, those aged 45-49 are welcome to participate in government-funded fecal occult blood screening to take charge of their own health. From now until August 31st, Monday to Friday between 8:30 AM and 11:30 AM, you can visit our office to pick up a collection tube. For inquiries, please call: 0981-768-19 - Yingge Health Center cares about you."

Recruitment: Participants will be identified through the health department's information system, which contains records of residents eligible for the national colorectal cancer screening program and their mobile phone numbers. There is no separate recruitment or enrollment procedure.

•Sample Size: A total of 6,708 eligible residents will be randomly assigned to the intervention and control groups. The sample size is calculated based on previous research, which indicates that approximately 13.1% of individuals in this age group participate in FOBT screening without active intervention. The study aims to increase participation by 5%, reaching an 18% participation rate with SMS invitations.

Timeline: The study will be conducted over from August 5, 2025 to Sep 18, 2025.

Data Collection and Management:

  • The health department will provide a de-identified list of eligible residents, including a random code, gender, age, and mobile phone number. This information will be used for random assignment and statistical analysis.
  • Random assignment will be performed using computer-generated random numbers.
  • The SMS messages will be sent by a contracted SMS provider. The health department will provide the SMS provider with a secure file containing the random code and mobile phone number for each participant.
  • The SMS provider will provide data on message delivery status. The health department staff will record whether participants obtain the screening kit and whether they completed fecal occult blood test. This information will be provided to the principal investigator (PI) for analysis.

Outcome Measures:

•Primary Endpoint: Numbers of completed fecal occult blood test. Data Analysis: The primary analysis will be conducted using an intention-to-treat (ITT) approach, where all participants will be included in the analysis based on their assigned group, regardless of whether they received the intervention or completed the screening.

Ethical Considerations: The study has been designed to protect the privacy and confidentiality of participants. Data will be de-identified and stored securely. All personal data will be protected through anonymized coding and data encryption. SMS dissemination will be handled by a third-party vendor under confidentiality agreements, and no personally identifiable information will be shared beyond phone number use for message delivery. The project is funded through existing administrative cancer screening budgets, without external sponsorship. The study will comply with all relevant ethical guidelines and regulations.

Conditions
No Condition
Being tested
Active SMS Invitation
Keywords
Colorectal Cancer Screening, SMS (Short Message Service), Mobile Health (mHealth), Randomized Controlled Trial, Fecal Occult Blood Test (FIT)

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Active SMS InvitationOther

    Participants in this group will receive a text message inviting them to participate in the free FOBT program. The SMS message will include a brief explanation of the program, instructions on how to obtain a screening kit, and a contact number for inquiries. A reminder SMS message will be sent one week after the initial message.

Study groups in NCT07112729
Study groupRoleWhat they receive
Intervention Group (Active SMS Invitation)ExperimentalParticipants in this group will receive a text message inviting them to participate in the free FOBT program. The SMS message will include a brief explanation of the program, instructions on how to obtain a screening kit, and a contact number for inquiries. A reminder SMS message will be sent one week after the initial message.
Receives: Other: Active SMS Invitation
Control GroupNo interventionParticipants in this group will receive the standard notification procedures typically used to inform residents about the FOBT program. After one month of the first SMS sent to the Intervention Group, the Control group will receive the same SMS message as the intervention group.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Primary Outcome

    Number of participants who Completed the fecal occult blood test. The date after SMS invitation of FIT completed was collected for evaluation with observed period (31 days).

    Measured: From first SMS to 31 days

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted8 Aug 2025
  2. Study start7 Aug 2025
  3. Primary completion4 Sep 2025
  4. Study completion18 Sep 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Health services research
Allocation
Randomised
Intervention model
Parallel groups
Model description
* Intervention Group (Active SMS Invitation): Participants in this group will receive a text message inviting them to participate in the free FOBT program. The SMS message will include a brief explanation of the program, instructions on how to obtain a screening kit, and a contact number for inquiries. A reminder SMS message will be sent one week after the initial message. * Control Group (Standard Notification): Participants in this group will receive the standard notification procedures typically used to inform residents about the FOBT program. After one month of the first SMS sent to the Intervention Group, the Control group will receive the same SMS message as the intervention group.
Masking
None (open label)
Enrolment
6,708 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07112729
Sponsor's protocol ID
202500921B0
Acronym
SMS
Status last verified
Jan 2026
First submitted
2 Aug 2025
Last updated
3 Feb 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: Based on research collaboration, de-identified participant-level results can be required from Principal Investigator.

Questions about this trial

What is this clinical trial studying?

A study testing Active SMS Invitation in people with No Condition, run by Chang Gung University at 1 site in Taiwan.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 3 Feb 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Taiwan. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Primary Outcome (time frame: From first SMS to 31 days). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 3 Feb 2026.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in