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Clinical Trials/NCT02828189
NCT02828189
Completed
Not Applicable

Efficacy of Therapeutic Exercise in Modulating Cancer-Related Fatigue in Women After Breast Cancer Treatment

University of Alcala1 site in 1 country80 target enrollmentJuly 2016

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Fatigue
Sponsor
University of Alcala
Enrollment
80
Locations
1
Primary Endpoint
Subjective assessment of perception of fatigue.
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

The main objective of this study is to determine whether the proposed program of therapeutic exercise is effective in improving fatigue, more than the exercise unsupervised depending on their preferences, in women treated for breast cancer.

Detailed Description

Introduction: The prevalence of cancer-related fatigue in women treated for breast cancer is about 30% having significant effects in reducing their quality of life. There is evidence of the presence of sleep problems and immune response. Several studies claim that physical exercise is effective during and after treatment of the disease as it improves the quality of life, cardiorespiratory function, physical functioning and symptoms of fatigue although not always found significant differences between intervention groups exercises compared with a control group. Although the results of these studies are promising, generally present methodological biases as small sample size, absence of masking, heterogeneous groups, lack of monitoring short and long term and especially lack of specificity in relation to prescribed exercise ( frequency, intensity, time and type of exercise). Subjects and methods: A randomized clinical trial, the examiner being blinded unaware of the intervention group to which subjects were assigned. Participants will be randomly assigned to two groups: An experimental group, where the participants will be treated with Therapeutic Exercise; And a group where will be done Physical Exercise according their preferences. Pre-intervention, immediate post-intervention, 3 and 6 months assessments will be made. The selection criteria will be: Adult women treated for breast cancer, completed at least 6 months before, with persistent fatigue. All participants must understand and sign freely Informed Consent. Sample size: 40 women for each group. Data Analysis: A descriptive analysis of all variables was performed. It establish for all cases a confidence level of 95% (p \<0.05). The effectiveness was assessed by comparing the experienced change of the two groups in outcome variables between physical therapy examinations.

Registry
clinicaltrials.gov
Start Date
July 2016
End Date
January 2020
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Sponsor
University of Alcala
Responsible Party
Principal Investigator
Principal Investigator

Virginia Prieto Gómez

Teacher care and research in physiotherapy Unit. Department of Physiotherapy. University of Alcala.

University of Alcala

Eligibility Criteria

Inclusion Criteria

  • Women treated for breast cancer, completed at least 6 months before, with persistent fatigue.
  • Women who do not present contraindications for physiotherapy and physical exercise (infection, metastasis, loco regional recurrence, cardiopulmonary disorders).
  • Women who have read, understood and signed informed consent freely.

Exclusion Criteria

  • Women with cognitive limitations to understand the information provided, instructions for treatment and consent to their participation in the study.

Outcomes

Primary Outcomes

Subjective assessment of perception of fatigue.

Time Frame: 6 months

FACIT-FatigueScale (total score)

Secondary Outcomes

  • Distance in meters(6 months)
  • Pain Intensity(6 months)
  • Subjective assessment of perception of dyspnoea(6 months)

Study Sites (1)

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