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Impact of a cognitive behavioral program on the quality of life of men with urinary incontinence radical prostatectomy: a randomized clinical trial

Urinary incontinence and quality of life in men undergoing prostatectomy radical

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-3sstqg
Enrollment
Unknown
Registered
2020-03-05
Start date
2019-08-10
Completion date
Unknown
Last updated
2025-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Urinary incontinence

Interventions

The proposed protocol for the cognitive-behavioral program focuses on the early rehabilitation of UI, including educational guidelines based on physiological and pathophysiological aspects of UI, with
Behavioural
F04.754.137
H02.478.676.789

Sponsors

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior
Lead Sponsor
Coordenação de Aperfeiçoamento de Pessoal de Nível Superior
Collaborator

Eligibility

Sex/Gender
Male
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: In order to compose the sample, the following inclusion criteria will be adopted: Age equal or superior to 18 years; Diagnosis of prostate adenocarcinoma; Schedule for PR at the institution included in the study; Agree to participate in the research; Present clinical conditions physical and psychological to answer the questions asked by the researcher; To report locomotor capacity for pelvic floor strengthening exercises; Have a telephone landline or cell phone to follow the teaching program; To present cognitive capacity for participation - application of mini mental state examination BERTOLUCCI et al., 1994.

Exclusion criteria

Exclusion criteria: In order to compose the sample, the following exclusion criteria will be adopted: Participants presenting with spinal cord injury, diabetes mellitus, stroke, dementia, Alzheimer's disease, previous pelvic surgery, diseases with a probable repercussion on urinary control; Participants with a history of bladder and / or prostate surgery.

Design outcomes

Primary

MeasureTime frame
Control of urinary incontinence determined through the pad test, with a lower percentage of incontinents in the post-intervention.

Secondary

MeasureTime frame
Health-related quality of life assessed using the ICIQ-SF scale scores

Countries

Brazil

Contacts

Public ContactLívia Izidoro

Universidade Federal de Goiás

liviaresende.enf@gmail.com62998364562

Outcome results

None listed

Source: REBEC (via WHO ICTRP) · Data processed: Feb 13, 2026