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Clinical Trials/NCT05873036
NCT05873036RecruitingNot Applicable

Comparison of Aerobic Training and Progressive Resistance Training to Improve Functional Ability After Breast Cancer Surgery

Superior University1 site in 1 country74 target enrollmentStarted: April 1, 2023Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Enrollment
74
Locations
1
Primary Endpoint
Goniometer Tool

Study Overview

Brief Summary

To determine the effect of aerobic training and progressive resistance training to improve upper limb functional ability after breast cancer surgery

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Health Services Research
Masking
None

Eligibility Criteria

Ages
35 Years to 65 Years (Adult, Older Adult)
Sex
Female
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •a) Breast cancer female survivors eligible under 35-65 years complaining of cancer-related fatigue.
  • •b) Adjunctive radiotherapy or underwent surgery (lumpectomy or mastectomy), willing to participate will be included in the study.
  • •c) Shoulder pain d) Decreased ROM e) Primary unilateral BC, ALND, no distant metastases, no previous ALND on the contra lateral side f) No previous history of arm lymph edema

Exclusion Criteria

  • •a) Survivors with other concurrent metastasis anywhere else in the body, diagnosed case of any cardiac or respiratory condition, contra-indicated for exercise training (severe dyspnea, chest pain, severe nausea, ataxia, dizziness etc.) b) Any other neurological or recent musculoskeletal problems were excluded from the study.
  • •c) Bilateral mastectomy d) Adjunctive chemotherapy

Arms & Interventions

Aerobic Training

Other

Intervention: Aerobic Training (Diagnostic Test)

Progressive Resistance Training

Experimental

Intervention: Progressive Resistance Training (Diagnostic Test)

Outcomes

Primary Outcomes

Goniometer Tool

Time Frame: 6 Months

Numerical pain rating scale (NPRS)

Time Frame: 6 Months

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Muhammad Naveed Babur

Principal Investigator

Superior University

Study Sites (1)

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