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Comparison of AT & PR Training to Improve Functional Ability After Breast Cancer Surgery

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

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05873036
Enrollment
74
Registered
2023-05-24
Start date
2023-04-01
Completion date
2023-08-31
Last updated
2023-05-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast Cancer

Brief summary

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

Interventions

DIAGNOSTIC_TESTAerobic Training

Aerobic Training to Improve Functional Ability After Breast Cancer Surgery

DIAGNOSTIC_TESTProgressive Resistance Training

Progressive Resistance Training to Improve Functional Ability After Breast Cancer Surgery

Sponsors

Superior University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
35 Years to 65 Years
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

Design outcomes

Primary

MeasureTime frame
Numerical pain rating scale (NPRS)6 Months
Goniometer Tool6 Months

Countries

Pakistan

Contacts

Primary ContactShama Zahid, DPT
dptm-f18-172@superior.edu.pk+923134432808

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026