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PFMT Educational Intervention for Patients With Advancer Breast Cancer

Pelvic Floor Muscle Training Educational Intervention for Patients With Breast Cancer

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04953377
Enrollment
42
Registered
2021-07-08
Start date
2021-09-02
Completion date
2023-04-10
Last updated
2023-03-24

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

Conditions

Advanced Breast Cancer

Keywords

pelvic floor muscle training, urinary incontinence, educational intervention

Brief summary

A PFMT educational intervention was designed for women with metastasic breast cancer. It consisted in a 120 min workshop and 8 weeks of non-supervised (but with follow-up) self-training. ICIQ, IQOL and ad hoc questions were performed before the workshop and after the 8 weeks training to see the prevalence of UI, the impact in their quality of life and the empowerment of self-training.

Detailed description

Urinary incontinence (UI) affects women of all ages and has a great impact on the quality of life. Cancer treatments such as chemotherapy or hormone therapy may play an important rol in the development and worsening of pelvic floor disorders. Little evidence on the prevalence and impact of UI in metastassis breast cancer women is known. A protocol was designed to analyze the effect of a PFMT educational intervention on the UI and the impact on the QoL, as well as in the empowerment feeling of the participants. Feasibility of the protocol will be analized to design an optimal RCT for testing our hypothesis During the usual visits, oncologist wil recruit women with advanced breast cancer who meet the inclusion criteria for the participation.

Interventions

BEHAVIORALPFMT educational intervention

an educational intervention to learn about the pelvic floor and how to train it

Sponsors

Onkologikoa
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Advanced breast cancer * Over 18 years old * ECOG≤2 * No inestable bone metastasis * life expentancy\>6 months * Literate in spanish

Exclusion criteria

* Physical exercise contraindications * Intense pain * Being pregnant

Design outcomes

Primary

MeasureTime frameDescription
Prevalence of urinary incontinencebaselineBy the ICIQ-UI Short Form, which is a questionnaire for evaluating the frequency, severity and impact on quality of life (QoL) of urinary incontinence in men and women in research and clinical practice across the world. It has 4 items, and the scoring scale is 0-21.
Feasibility-Quantitative and qualitative retention log8 weeksInformation about number of participants who dropped out, and reason for drop-out
Feasibility- Adherence to the program8 weeksAdherence will be difined as the percentage of completed weeks of training out of 8 weeks. A week will be considerered valid when the train was performed at least in 2 different days.
Feasibility- Satisfaction with the workshopbaselineA satisfaction 9 item questionnaire was design (Scale 1-5) to obtain information about the satisfaction with the (1) duration, (2) the content, (3) explanations, (4) atmosphere (5)number of participants during the workshop and (6) the importance for other patients to access this information, (7) increase in knowledge, (8) knowledge to train alone and (9) overall satisfaction.
Feasibility- Recruitment rates8 weeksNumber of patients enrolled divided by number of patients eligible
Feasibility - Qualitative analyses of recruitment8 weeksQualitative information regarding recruitment and reasons for patients not participating will be collected in the researchers log

Secondary

MeasureTime frameDescription
Impact of urinary incontinence on the quality of life8 weeksThe I-QOL measures the effect of urinary incontinence on quality of life.It is divided into 3 subscales: Avoidance and limiting behavior, Psychosocial impact, and Social embarrassment (SE). Subjects use a 5-point response scale with values ranging from 1 (extremely) to 5 (not at all)
Knowledge and empowerment8 weeksA 11 item questionnaire was designed to analyse the population's initial knowledge of pelvic floor health and compare it with the knowledge maintained after the intervention. 5-point scale (0-4).
Changes in urinary incontinence8 weeksBy the ICIQ-UI Short Form, which is a questionnaire for evaluating the frequency, severity and impact on quality of life (QoL) of urinary incontinence in men and women in research and clinical practice across the world. It has 4 items, and the scoring scale is 0-21.

Countries

Spain

Contacts

Primary ContactMireia Pelaez, PhD
mpelaez@onkologikoa.org+34943838284

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026