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Effect of Kinesiotaping Augmented By Resistive Exercise on Fatigue, Physical Strength, Quality of Life in Breast Cancer Survivors

Not Applicable
Not yet recruiting
Conditions
Breast Cancer
Quality of Life
Fatigue
Interventions
Other: resistive training
Other: kinesiotaping
Registration Number
NCT05726643
Lead Sponsor
Cairo University
Brief Summary

The purpose of the study will be to investigate the effect of kinesotaping augmented by resistive exercise on fatigue, muscle strength, and QoL in breast cancer survivors.

Detailed Description

The present study will provide an evidence base to women's health care providers about the effect of strength training augmented by kinesotaping on fatigue, QoL and muscle strength in breast cancer women compared to strength training alone

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
All
Target Recruitment
40
Inclusion Criteria
  • Patient's age will range from 40- 55 years.
  • Their body mass index (BMI) will be from 25 to 29,9 Kg/m2.
  • They suffer from breast cancer.
  • They will receive chemotherapy within previous 3 months.
  • They complain from fatigue, deterioration in their daily living activity (ADL) and feeling of weakness in their muscles.
Exclusion Criteria
  • Respiratory or heart problems affecting mobility
  • Marked skeletal deformity.
  • Visual system affection.
  • Cognition problems.
  • Previous surgeries at their back and/or lower limbs.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
kinesotaping groupkinesiotapingconsists of 20 patients who will receive resistive training program augmented by kinesotaping, 2 times /week for 12 weeks.
resistive training groupresistive trainingconsists of 20 patients who will receive resistive training for 2times per week for 12 weeks
kinesotaping groupresistive trainingconsists of 20 patients who will receive resistive training program augmented by kinesotaping, 2 times /week for 12 weeks.
Primary Outcome Measures
NameTimeMethod
Assessing the change in fatigueat baseline and after 12 weeks of intervention

The Fatigue Severity Scale is a 14-item will be used to measure the severity, frequency and diurnal variation of fatigue, as well as its perceived interference with quality of life.

Assessing the change in quality of lifeat baseline and after 12 weeks of intervention

By using 36-Item Short Form (SF-36) health survey will be used to assess QoL. The SF-36 questionnaire includes eight multiple-item subscales that evaluate physical function, social functioning, role limitations due to physical problems and role limitations due to emotional problems, mental health, vitality, pain and general health perception. Total score on each SF-36 subscale ranges between 0 and 100. Greater score indicates better QoL

Assessing the change in muscle strengthat baseline and after 12 weeks of intervention

Muscle strength will be assessed using dynamometer at starting and after 12 weeks of the treatment course.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Outpatient clinic faculty of physica therapy cairo university

🇪🇬

Dokki, Egypt

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