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RUTISS-Diary and RUTISS-65 Study

NCT07698041 · Status: NOT_YET_RECRUITING · Type: OBSERVATIONAL · Enrollment: 200

Last updated 2026-07-13

No results posted yet for this study

Summary

Existing patient-reported outcome measures assess acute urinary tract infection but do not support daily symptom tracking in recurrent UTI (rUTI) or meet the needs of older adults. This single-site study will develop and validate two adapted measures: the RUTISS-Diary for daily symptom monitoring and the RUTISS-65 for reporting symptoms in adults aged 65 years and over. Approximately 200 participants with rUTI will complete the RUTISS-Diary daily for 7 days and again on day 14. Participants aged 65 years and over will also complete the RUTISS-65 on days 1 and 2 to assess its reliability and validity.

Conditions

  • Urology
  • Urological Diseases
  • Patient Satisfaction
  • Pain, Chronic

Interventions

OTHER

Non-interventional Patient Reported Outcome Measure Development (RUTISS-Diary)

RUTISS-Diary

OTHER

Non-interventional Patient Reported Outcome Measure Development (RUTISS-65)

RUTISS-65

Sponsors & Collaborators

  • Royal Berkshire NHS Foundation Trust

    collaborator OTHER_GOV

  • Katherine Finlay

    lead OTHER

Principal Investigators

  • Katherine A Finlay, PhD, CPsychol · University of Reading

  • Bob Yang, FRCS (UROL), MBBS, BSC (HONS) · Royal Berkshire NHS Foundation Trust

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-07-08
Primary Completion
2027-06-30
Completion
2027-12-24

Countries

  • United Kingdom

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07698041 on ClinicalTrials.gov