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临床试验/NCT06527638
NCT06527638进行中(未招募)不适用

PURI-PRO (Portuguese URinary Incontinence PROject) - Symptoms Impact and eHealth Intervention for Menopausal Women With Urinary Incontinence

ISPA - Instituto Universitario de Ciencias Psicologicas, Sociais e da Vida1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2025年4月22日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
80
试验地点
1
主要终点
Brief Assessment of Urinary Incontinence symptoms and impact of Quality of Life

研究概览

简要总结

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.

详细描述

PURI-PRO's 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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
Single (Participant)

入排标准

年龄范围
40 Years 至 65 Years(Adult, Older Adult)
性别
Female
接受健康志愿者
是

入选标准

  • •Age (40-65 years);
  • •Sex (women);
  • •The presence of UI (positive response to a question about experiencing involuntary urine loss during intra-abdominal pressure increment and/or when feeling an incontrollable urge to urinate, occasionally or frequently);
  • •Internet access.

排除标准

  • •Pregnancy or delivery in the past 6 months;
  • •Previous UI-related surgery;
  • •History of pelvic prolapse:
  • •Known malignancy in the lower abdomen;
  • •Neurological disease that could affect bladder control;
  • •Substance use disorder.

研究组 & 干预措施

eHealth intervention for UI symptoms improvement

Experimental

Participants in the Experimental Group were integrated into an eHealth 8-week group intervention, based on the Health Action Process Approach (HAPA).

The eHealth (internet-based) cognitive-behavioural intervention developed to promote UI symptoms improvement consisted of: i) weekly group sessions (by Zoom platform), with a specific theme in each session, ii) weekly challenges, and iii) WhatsApp group interaction.

干预措施: Experimental Group: eHealth intervention for UI symptoms improvement (Behavioral)

Control Group: Delivery of a Health Literacy single-leaflet

Active Comparator

The control group received a health literacy single-leaflet, delivered through email.

干预措施: Control Group: Delivery of a Health Literacy single-leaflet (Behavioral)

结局指标

主要结局

Brief Assessment of Urinary Incontinence symptoms and impact of Quality of Life

时间窗: Change from Baseline urinary incontinence symptoms and impact on quality of life adherence to mid-intervention (1 month later), post-intervention (2 months later), and at a 3 month follow-up

Evaluated by "International Consultation on Incontinence Questionnaire-Urinary Incontinence Short Form" (ICIQ-UI SF)

UI-related Coping Strategies

时间窗: Change from Baseline UI-related coping strategies to mid-intervention (1 month later), post-intervention (2 months later), and at a 3 month follow-up

Evaluated by a bi-factorial instrument (hiding coping dimension and defensive coping dimension) developed by our team that entails a set of UI-related maladaptive coping strategies to manage immediate effects of UI. This instrument is based on the work of Diokno and collaborators.

UI-related Beliefs

时间窗: Change from Baseline UI-related beliefs to mid-intervention (1 month later), post-intervention (2 months later), and at a 3 month follow-up

Evaluated by the Portuguese version of the "Brief Illness Perception Questionnaire" (IPQ-Brief). This instrument is based on the work of Figueiras and collaborators.

次要结局

  • Urinary Incontinence symptom severity and impact(Change from Baseline Urinary Incontinence symptom severity and impact to mid-intervention (1 month later), post-intervention (2 months later), and at a 3 month follow-up)
  • Self-reported Quality of Life(Change from Baseline quality of life to mid-intervention (1 month later), post-intervention (2 months later), and at a 3 month follow-up)
  • Behavior Change (HAPA)(Change from Baseline behavior to mid-intervention (1 month later), post-intervention (2 months later), and at a 3 month follow-up)
  • Self-esteem(Change from Baseline self-esteem to mid-intervention (1 month later), post-intervention (2 months later), and at a 3 month follow-up)
  • Social Isolation(Change from Baseline social isolation to mid-intervention (1 month later), post-intervention (2 months later), and at a 3 month follow-up)
  • Pelvic Floor and UI Knowledge(Change from Baseline pelvic floor and UI knowledge to mid-intervention (1 month later), post-intervention (2 months later), and at a 3 month follow-up)
  • Pelvic Floor Muscle Exercises Adherence(Change from Baseline pelvic floor muscle exercises adherence to mid-intervention (1 month later), post-intervention (2 months later), and at a 3 month follow-up)

研究者

发起方
ISPA - Instituto Universitario de Ciencias Psicologicas, Sociais e da Vida
申办方类型
Other
责任方
Principal Investigator
主要研究者

Marta Monteiro da Silva Gonçalves Porto

Principal Investigator

ISPA - Instituto Universitario de Ciencias Psicologicas, Sociais e da Vida

研究点 (1)

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