Viewing Study NCT06527638



Ignite Creation Date: 2024-10-26 @ 3:36 PM
Last Modification Date: 2024-10-26 @ 3:36 PM
Study NCT ID: NCT06527638
Status: ACTIVE_NOT_RECRUITING
Last Update Posted: None
First Post: 2024-07-17

Brief Title: PURI-PRO - Symptoms Impact and eHealth Intervention for Menopausal Women With Urinary Incontinence
Sponsor: None
Organization: None

Study Overview

Official Title: PURI-PRO Portuguese URinary Incontinence PROject - Symptoms Impact and eHealth Intervention for Menopausal Women With Urinary Incontinence
Status: ACTIVE_NOT_RECRUITING
Status Verified Date: 2024-10
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: PURI-PRO
Brief Summary: 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 202005710BD 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
Detailed Description: PURI-PROs intervention followed an experimental design randomised controlled trial involving UI intervention Experimental Group-EG vs Health Literacy single-leaflet Control Group-CG both delivered through the internet eHealth The study was comparative since the sample was distributed in two groups EG vs CG through randomised distribution and longitudinal since all the outcome measures were evaluated at four different times

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None