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NCT Number: NCT07516912

Evaluation of Free STI Testing Pilot Projects in Lucerne and Zurich, Switzerland

The main goal of the observational study is to evaluate participants' satisfaction with free HIV and sexually transmitted infection (STI) testing and counselling offered by the cities of Lucerne and Zurich, Switzerland to young people and people with low incomes. Counselling and testing can be accessed without participating in the study arm of the project.

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Key information

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • taking part in the pilot programmes
  • understand the study information
  • 16 years of age or older

Exclusion criteria

  • not eligible for the pilot programmes
  • not understanding the study information
  • less than 16 years old

Treatment and study plan

Primary outcomes

  1. Participants' satisfaction (study-specific satisfaction scale)

    Time frame: 3 years

    Participants' satisfaction is measured as the proportion of participants who "agree" or "strongly agree" with satisfaction statements in the post-visit questionnaire. 5-point Likert scale (1 = strongly disagree, 5 = strongly agree); higher scores indicate greater agreement, thus higher satisfaction.

Secondary outcomes

  1. Service capacity/utilisation

    Time frame: 3 years

    Number of completed voluntary counselling and testing visits recorded per month across participating sites.

  2. Access timeliness

    Time frame: 3 years

    Median number of days between booking date and appointment date for VCT visits

  3. Workload healthcare providers

    Time frame: 3 years

    Healthcare provider workload assessed via a short survey measuring perceived workload and time burden, assessed using a standardised Likert-type scale (1-5); higher scores indicate greater perceived workload.

  4. Count diagnosed HIV/STI cases

    Time frame: 3 years

    Number of newly diagnosed HIV and STI cases identified through the free voluntary counselling and testing visits across participating sites per reporting period.

  5. Number of treated STI cases

    Time frame: 3 years

    Number of participants who received an STI or HIV diagnosis during the pilot project and subsequently received treatment, defined as antibiotics dispensed at a pharmacy or attendance at a medical appointment at Maihof Praxis Lucerne or Checkpoint Zurich.

  6. Participants' perception of comfort regarding sexual health

    Time frame: 3 years

    Participant-reported comfort regarding sexual health (encompassing physical, emotional, and social wellbeing related to sexuality and relationships), measured on a visual analogue scale from 0 (not comfortable) to 100 (very comfortable). Filled in at clinic while waiting for appointment and again approximately 1 week after the appointment.

  7. Testing behaviour

    Time frame: 3 years

    Testing behaviour assessed via administrative data and self-report. Participants indicate whether this is their first STI/HIV test and, for HIV testing, time since last HIV test. Trends in testing frequency are monitored over the study period.

  8. Changes in sexual health topics familiarity

    Time frame: 3 years

    Participants rate 12 topics on a scale from 1 to 5 (1=never heard of it, 5=very familiar); higher scores indicate greater knowledge. Participants rate their familiarity at the clinic prior to the appointment and approximately 1 week after the appointment. The measure is the change between pre- and post-appointment rating.

  9. Changes in sexual health knowledge

    Time frame: 3 years

    Knowledge assessed using 8 true/false items (total score range: 0-8), administered at the clinic prior to the appointment and again approximately one week post-appointment. Higher scores indicate greater knowledge. The measure is the change in score from pre- to post-appointment.

  10. Changes in self-efficacy/attitudes

    Time frame: 3 years

    Self-efficacy and attitudes assessed using 13 items rated on a 5-point Likert scale (1 = strongly disagree, 5 = strongly agree), administered at the clinic prior to the appointment and again approximately one week post-appointment. Higher scores indicate greater self-efficacy and more positive attitudes. The measure is the change in score from pre- to post-appointment.

  11. Information-seeking behaviour

    Time frame: 3 years

    Information-seeking behaviour is assessed using a multiple-choice question identifying sources of sexual health information (e.g., internet, healthcare provider, peers). Reported descriptively as frequency and distribution of sources selected; administered at the clinic prior to the appointment only.

  12. Proportion of low-income eligible participants

    Time frame: 3 years

    Proportion of participants holding a KulturLegi card (indicating low-income eligibility) among all enrolled participants; reported descriptively.

  13. Reach Among Low-Income Eligible Population

    Time frame: 3 years

    Proportion of KulturLegi card holders enrolled in the study relative to the total number of KulturLegi cards issued in the catchment area during the study period. Assessed by comparing observed reach against a pre-specified target of ≥5% of the eligible low-income population.

  14. Comparative Outcomes by Eligibility Group

    Time frame: 3 years

    STI/HIV positivity rates, re-testing rates, and knowledge scores compared between low-income eligible participants (KulturLegi card holders) and age-eligible participants. Differences between groups are reported descriptively; regression modelling may be applied to explore associations and inform policy decisions.

Study contacts

Contact information is provided by the study sponsor or research team.

Andrea C Farnham, PhD

CONTACT

[email protected]

+41 44 634 60 00

Sponsors and collaborators

Lead sponsor

University of Zurich

Other

Collaborators

  • Checkpoint Lucerne
  • Checkpoint Zurich
  • Test-In Zurich

Registry information

Official study title

feSTI: Evaluation of Free HIV and STI Testing and Counselling Services for Young and Disadvantaged Populations in Lucerne and Zurich

Acronym: feSTI

Important dates

Study start
2026
Primary completion
2028
Study completion
2029
First posted
Apr 8, 2026
Registry last updated
Apr 8, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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