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Effects of exercise in the perineal region through the use of an application in pregnant women

Effects of pelvic floor muscle training with mobile app in pregnant women

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-4nzjmt
Enrollment
Unknown
Registered
2018-12-18
Start date
2019-03-01
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

Pelvic Floor muscle

Interventions

The study included 84 primiparous women from 16 weeks of gestation, healthy, aged over 18 years, who will be randomly divided into 3 groups: TMAP_convencional group (n = 28) composed of pregnant women
E02.779

Sponsors

Universidade Federal de Uberlândia
Lead Sponsor
Universidade Federal de Uberlândia
Collaborator

Eligibility

Sex/Gender
Female
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: Age over 18 years; Gestational age of 16 weeks gestational; Primiparae; Presence of pelvic lining muscle strength greater than 2 by the Modified Oxford Scale; Medical authorization for physical therapy intervention; Own the mobile device with android system; • Own the mobile device with android system; Have an understanding of the functioning of the application developed by the research team; Have internet when downloading the application and for the call center; Understand the use of the platform used for the call center

Exclusion criteria

Exclusion criteria: Multiple gestation; Presence of bone deformities, important muscular and nervous dysfunctions; Presence of high gestational risk; Perform previous pelvic floor muscle training;; Lower urinary tract infection

Design outcomes

Primary

MeasureTime frame
Pelvic Floor Muscle Strength, verified by PeritronTM brand electronic pressure gauge, pre, six weeks and post intervention.

Secondary

MeasureTime frame
The sexual function will be evaluated through the application of the Female Sexual Function Scale (FSFI), in the periods of pre, six weeks and post intervention.;The complaint of urinary loss will be evaluated through the International Consultation on Incontinence Questionnaire - Short Form (ICIQ-SF), in the periods of pre, six weeks and post intervention.;The satisfaction of the intervention received will be evaluated through an application that will be developed by the researchers. This instrument will focus on the opinion of the volunteers regarding the service offered, being registered through the visual analogue scale in which they will graduate the opinion in bad, regular, good and great, at each end of the intervention session.

Countries

Brazil

Contacts

Public ContactVanessa Pereira Baldon

Universidade Federal de Uberlândia

pereiravans@gmail.com+55-034-32182935

Outcome results

None listed

Source: REBEC (via WHO ICTRP)