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Clinical Trials/NCT06215027
NCT06215027
Recruiting
Not Applicable

Os Efeitos da dança Como Recurso terapêutico em Pacientes Com câncer de Mama Submetidas a Tratamento cirúrgico

AC Camargo Cancer Center1 site in 1 country30 target enrollmentFebruary 1, 2024
ConditionsBreast Cancer

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Breast Cancer
Sponsor
AC Camargo Cancer Center
Enrollment
30
Locations
1
Primary Endpoint
ROM
Status
Recruiting
Last Updated
last year

Overview

Brief Summary

The goal of this non randomized clinical trial, with pre- and post-intervention evaluation, longitudinal, with prospective data collection is to evaluate the effects of dance as a therapeutic intervention in breast cancer patients undergoing surgical treatment.

Detailed Description

The hypothesis is that dance will promote improvements in range of motion, strength, fatigue, functionality, pain and quality of life for breast cancer patients undergoing surgical treatment. Objectives: To evaluate the effects of dance as a therapeutic intervention in breast cancer patients undergoing surgical treatment on: shoulder range of, overall muscle strength, fatigue, respiratory muscle strength, functionality, pain and quality of life. Method: This is a non-randomized randomized clinical trial, with pre- and post-intervention evaluation, prospective data collection. The following will be used for pre-intervention assessment: goniometry, dynamometry, manovacuometry, 6-minute walk test, fatigue and quality of life questionnaire, and quality of life questionnaire, as well as a pain assessment scale. After 16 weeks, the same variables will be assessed.

Registry
clinicaltrials.gov
Start Date
February 1, 2024
End Date
May 30, 2026
Last Updated
last year
Study Type
Interventional
Study Design
Single Group
Sex
Female

Investigators

Sponsor
AC Camargo Cancer Center
Responsible Party
Principal Investigator
Principal Investigator

Leticia Zumpano Cardenas

PHD, physiotherapist at the intensive care unit, stricto sensu postgraduate professor

AC Camargo Cancer Center

Eligibility Criteria

Inclusion Criteria

  • patients diagnosed with breast cancer
  • undergone surgical resection
  • after medical referral for physiotherapy
  • and physiotherapeutic assessment

Exclusion Criteria

  • patients with another previous oncological diagnosis
  • previous neuromuscular diseases
  • patients who do not agree to take part in the study
  • or the impossibility of carrying out the muscle strength assessment and/or other assessments

Outcomes

Primary Outcomes

ROM

Time Frame: Pre-intervention and after 16 weeks

Shoulder range of motion

Secondary Outcomes

  • Overall muscle strength(Pre-intervention and after 16 weeks)
  • respiratory muscle strength(Pre-intervention and after 16 weeks)
  • Functionality(Pre-intervention and after 16 weeks)
  • Pain intensity(Pre-intervention and after 16 weeks)
  • Fatigue(Pre-intervention and after 16 weeks)
  • Quality of life (physical well-being, social and family well-being, emotional well-being, functional well-being)(Pre-intervention and after 16 weeks)

Study Sites (1)

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