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PURI-PRO - Symptoms Impact and eHealth Intervention for Menopausal Women With Urinary Incontinence

Study acronym: PURI-PRO
StatusActive, Not Recruiting
PhaseNot applicable
Started
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Record status
This record was last updated December 15, 2025 (before its estimated December 18, 2025 completion). Its status may not reflect the trial's current state.

Record History

See every version on ClinicalTrials.gov ↗

  1. Trial status: Recruiting to Active, Not Recruiting
    • Primary completion date: Jul 18, 2025 to Dec 18, 2025
    • Study completion date: Oct 18, 2025 to Jan 2026
    • Site details revised
    v11
  2. Re-verified, no change to tracked fieldsv10
  3. Start date: Mar 6, 2024 to Apr 22, 2025
    • Primary completion date: May 30, 2025 to Jul 18, 2025
    • Study completion date: Jul 25, 2025 to Oct 18, 2025
    v9
  4. Trial status: Active, Not Recruiting to Recruiting
    • Primary completion date: May 12, 2024 to May 30, 2025
    • Study completion date: Mar 12, 2025 to Jul 25, 2025
    • Site details revised
    v8
  5. Re-verified, no change to tracked fieldsv7
Show 5 earlier versionsHide 5 earlier versions
  1. Primary endpoints: 2 to 3
    • Secondary endpoints: 8 to 7
    v6
  2. Primary endpoints: 3 to 2
    • Study completion date: Oct 12, 2024 to Mar 12, 2025
    • Secondary endpoints: 7 to 8
    v5
  3. Eligibility criteria expanded, about 10 words
    • Secondary endpoints: details revised at 1 of 7 entries
    • Publications revised (24)
    v4
  4. Re-verified, no change to tracked fieldsv3
  5. Secondary endpoints: details revised at 7 of 7 entriesv2
  1. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
Urinary Incontinence (UI) is a public health problem that disrupts the Quality of Life, Productivity, Social Isolation and Sexual Function; its prevalence in peri- and postmenopausal women is around 30-40%. UI remains underreported and undertreated. Previous eHealth interventions have been efficacious with women. Thus, PURI-PRO (Portuguese Urinary Incontinence Project) (FCT Grant 2020.05710.BD) entailed a low-cost 8-week eHealth cognitive-behavioural multidisciplinary intervention aimed at reducing UI symptoms' severity through Pelvic Floor Muscle Training, development of healthy bladder habits, and promotion of adherence to exercises, realistic UI-beliefs, and functional coping strategies. Urinary incontinence symptom severity, frequency and its impact on quality of life, beliefs and strategies regarding urinary incontinence, self-esteem, social isolation, and adherence to pelvic floor muscle excercises were evaluated.
Trial Details
NCT Number NCT06527638
Lead Sponsor ISPA - Instituto Universitario de Ciencias Psicologicas, Sociais e da Vida
Collaborators: Fundação para a Ciência e a Tecnologia
Conditions
(from sponsor)		 Urinary Incontinence
Related terms Social Isolation, Urinary Incontinence
Enrollment 80 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov