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Profile of patients with fecal leakage and suggestion of physiotherapeutic treatment for patients with bowel complaints and leakage of feces

Conditions
Fecal Incontinence
Constipation
A01.923.600.600
Registration Number
RBR-65zd2v4
Lead Sponsor
Faculdade de Medicina da Universidade de São Paulo
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Data analysis completed
Sex
Female
Target Recruitment
Not specified
Inclusion Criteria

Study group: patients with complaints of constipation and patients with fecal incontinence; in the control group und without pelvic dysfunctions; everyone over 18 years old; who signed the Free and Informed Consent Term (ICF).

Exclusion Criteria

Individuals with cognitive impairment; individuals without constipation and fecal incontinence in the study group; in the control group individuals who had pelvic complaints. In both groups, individuals with: untreated respiratory diseases, visual alteration (without correction), acute vestibular and orthopedic alterations, practice of intense physical exercise (athletes).

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Expected outcome 1 - Phase I of the study: information about personal and clinical data of both groups, about comorbidities, pathological, surgical and functional history.;Expected outcome 2 - Phase I: Observation of evaluative measures of respiratory pressures and balance measures of the groups;Outcome found 2 - Phase 1: Patients in the study group have greater medio-lateral postural sway in the semi-static posture in the condition with reduced proprioceptive afferent and in the assessment of breathing, lower values were observed in relation to respiratory muscle strength when compared to healthy individuals.;Outcome found 1 - There was a greater number of comorbidities in the study group and an important frequency in relation to perineal surgery, a possible cause of the dysfunction. Other possible causes were present, such as obstetric trauma, but both groups were present. Complaints of falls and dyspnea were also more frequent in the study group.
Secondary Outcome Measures
NameTimeMethod
Expected outcome 1 - Phase 2: After intervention, improvement is expected in relation to the results of clinical tests performed through manovacuometry, force platform and measured questionnaires to verify respiratory muscle strength and postural balance in the study group and in the control group, with variables measured by relative frequency , absolute and comparative tests.
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