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Testicular CancerNCT07841041

Effects of Testicular Self-Examination Training Methods on Students' Behaviors and Health Beliefs

A study testing Educational Brochure and Audio Recording and Educational Brochure in people with Testicular Cancer and Testicular Self-Examination, run by Yeditepe University at 1 site in Turkey (Türkiye).

Completed

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

Official record
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Trial summary

The goal of this cluster randomized controlled trial is to evaluate and compare the effects of different testicular self-examination (TSE) training methods on university students' health beliefs and self-examination behaviors regarding testicular cancer (TC) and TSE. Read more about this study

Who is it for?
Ages 18 years and older, men onlyHealthy volunteers can take part
What is being tested?
Educational Brochure and Audio Recording and Educational Brochure
Could I receive a placebo?
No, everyone receives an active treatment
How many people
122 participants
Where
1 siteTurkey (Türkiye)
Study dates
6 Jan 2025to 5 Jan 2026
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 18 years and older
  • Men only
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • Being biologically male
  • Being an active university student enrolled at the university
  • Being aged 18 years or older
  • Having native or fluent Turkish literacy (reading and writing)
  • Having access to a technological device (smartphone, computer, or tablet) with an active internet connection to access digital materials and surveys
  • Voluntary agreement to participate in the study and providing informed consent

Who cannot join

  • Previous clinical diagnosis of testicular cancer or any other testicular/scrotal malignancy
  • Having undergone major scrotal or testicular surgery (e.g., orchiectomy)
  • Prior formal or professional training on testicular self-examination (TSE) within the last 6 months
  • Inability to complete the educational intervention or follow-up assessments due to sensory or cognitive impairments

Trial locations and contacts

1 site in 1 country.

Turkey (Türkiye)1 site
  • Yeditepe University

    Istanbul

Other trials in Turkey (Türkiye)

About this study

Official title: Comparison of the Effects of Testicular Self-Examination Training Methods on Students' Behaviors and Health Beliefs Regarding Testicular Cancer and Testicular Self-Examination: A Randomized Controlled Trial

The goal of this cluster randomized controlled trial is to evaluate and compare the effects of different testicular self-examination (TSE) training methods on university students' health beliefs and self-examination behaviors regarding testicular cancer (TC) and TSE.

The main questions it aims to answer are:

Read more
  • Does receiving brochure-based education or brochure plus audio recordings of TC patient experiences improve students' health beliefs (perceived susceptibility, seriousness, benefits, self-efficacy, and reduced barriers)?
  • Which educational method is more effective in increasing the frequency and performance of testicular self-examination behaviors compared to a control group?

Researchers will compare three groups:

  • Intervention Group 1: Receives an educational brochure on TC and TSE.
  • Intervention Group 2: Receives an educational brochure combined with audio recordings of testicular cancer survivor/patient experiences.
  • Control Group: Receives no specific educational intervention during the study period.

Participants will:

  • Complete baseline questionnaires regarding demographic information, TC/TSE knowledge, health beliefs, and baseline examination practices.
  • Receive the assigned educational material/session according to their randomized cluster.
  • Complete follow-up evaluations at 3 months post-intervention to assess changes in health beliefs, knowledge, and TSE behaviors.
Being tested
Educational Brochure and Audio Recording, Educational Brochure, Control Group
Medical subject headings
Testicular Neoplasms, Health Behavior, Behavior

What participants receive

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

  • Educational Brochure and Audio RecordingBehavioural

    Following face-to-face recruitment, obtaining informed consent, and collecting phone numbers from eligible university students, pre-tests-including the Introductory and Testicular Self-Examination (TSE) Characteristics Form along with Champion's Health Belief Model Scale-were administered online via Google Forms via WhatsApp (approximate completion time: 15 minutes). At the end of the sixth week following the pre-test, the brochure and audio-recorded experience-sharing intervention group received their respective protocol, followed by post-tests comprising the TSE Behavior Determination Form and the TSE Behavior and Educational Tool Satisfaction Form.

  • Educational BrochureBehavioural

    Following face-to-face recruitment, obtaining informed consent, and collecting phone numbers from eligible university students, pre-tests-including the Introductory and Testicular Self-Examination (TSE) Characteristics Form along with Champion's Health Belief Model Scale-were administered online via Google Forms via WhatsApp (approximate completion time: 15 minutes). At the end of the sixth week following the pre-test, the educational brochure intervention group received their respective protocol, followed by post-tests comprising the TSE Behavior Determination Form and the TSE Behavior and Educational Tool Satisfaction Form.

  • Control GroupOther

    Following face-to-face recruitment, obtaining informed consent, and collecting phone numbers from eligible university students, pre-tests-including the Introductory and Testicular Self-Examination (TSE) Characteristics Form along with Champion's Health Belief Model Scale-were administered online via Google Forms via WhatsApp (approximate completion time: 15 minutes). For the control group, no active educational intervention was administered following the pre-test, and only the TSE Behavior Determination Form was applied as a post-test at the end of the sixth week.

Study groups in NCT07841041
Study groupRoleWhat they receive
Intervention 2 (Educational Brochure Group)ExperimentalFollowing face-to-face recruitment, obtaining informed consent, and collecting phone numbers from eligible university students between, pre-tests-including the Introductory and Testicular Self-Examination (TSE) Characteristics Form along with Champion's Health Belief Model Scale-were administered online via Google Forms via WhatsApp (approximate completion time: 15 minutes). At the end of the sixth week following the pre-test, the educational brochure group received their respective protocol, followed by post-tests comprising the TSE Behavior Determination Form and the TSE Behavior and Educational Tool Satisfaction Form.
Receives: Behavioral: Educational Brochure
Control Group (No Intervention)OtherFollowing face-to-face recruitment, obtaining informed consent, and collecting phone numbers from eligible university students, pre-tests-including the Introductory and Testicular Self-Examination (TSE) Characteristics Form along with Champion's Health Belief Model Scale-were administered online via Google Forms via WhatsApp (approximate completion time: 15 minutes). For the control group, no active educational intervention was administered following the pre-test, and only the TSE Behavior Determination Form was applied as a post-test at the end of the sixth week.
Receives: Other: Control Group
Intervention 1 (Educational Brochure and Experience-Sharing Recordings Group)ExperimentalFollowing face-to-face recruitment, obtaining informed consent, and collecting phone numbers from eligible university students, pre-tests-including the Introductory and Testicular Self-Examination (TSE) Characteristics Form along with Champion's Health Belief Model Scale-were administered online via Google Forms via WhatsApp (approximate completion time: 15 minutes). At the end of the sixth week following the pre-test, the educational brochure and audio-recorded experience-sharing intervention group received their respective protocol, followed by post-tests comprising the TSE Behavior Determination Form and the TSE Behavior and Educational Tool Satisfaction Form.
Receives: Behavioral: Educational Brochure and Audio Recording

What is being measured

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

  1. Change in Testicular Self-Examination (TSE) Behavior

    Measured using the TSE Behavior Determination Form to evaluate whether the students perform regular testicular self-examination.

    Measured: At baseline and at 6 weeks post-intervention

Secondary outcomes (1)
  1. Change in Champion's Health Belief Model Scale Scores

    Evaluated using Champion's Health Belief Model Scale to assess changes in students' health beliefs regarding testicular self-examination between the intervention groups and the control group. Champion's Health Belief Model Scale (CHBMS), consisting of 26 items across five subscales (Perceived Susceptibility, Perceived Severity, Perceived Benefits, Perceived Barriers, and Perceived Self-Efficacy) scored on a 5-point Likert scale (1 to 5). The scale does not yield a total score; each subscale is evaluated separately with varying score ranges depending on the number of items, where higher scores indicate a higher level of each specific health belief.

    Measured: At baseline and at 6 weeks post-intervention

Timeline

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

  1. First posted25 Sep 2026
  2. Study start6 Jan 2025
  3. Primary completion30 Sep 2025
  4. Study completion5 Jan 2026

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
Prevention
Allocation
Randomised
Intervention model
Parallel groups
Masking
Double blind
Who is masked
Participant, Outcomes assessor
Enrolment
122 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07841041
Sponsor's protocol ID
2024/12- 362602
Status last verified
Aug 2026
First submitted
20 Sep 2026
Last updated
6 Oct 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: De-identified individual participant data collected during the study will be available upon reasonable request directed to the corresponding author.

Questions about this trial

What is this clinical trial studying?

A study testing Educational Brochure and Audio Recording and Educational Brochure in people with Testicular Cancer and Testicular Self-Examination, run by Yeditepe University at 1 site in Turkey (Türkiye).

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 6 inclusion and 4 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 6 Oct 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 Turkey (Türkiye). 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?

Change in Testicular Self-Examination (TSE) Behavior (time frame: At baseline and at 6 weeks post-intervention). 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 6 Oct 2026.

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