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Comparing the efficacy of two different therapeutic interventions in post-mastectomy patients

Efficacy of Upper Trunk Proprioceptive Neuromuscular Facilitation in comparison with Complex Decongestive Therapy in post mastectomy patients - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/07/071186
Enrollment
30
Registered
2024-07-24
Start date
Unknown
Completion date
Unknown
Last updated
2024-08-19

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

Conditions

Health Condition 1: D249- Benign neoplasm of unspecified breast

Interventions

Intervention1: Complex Decongestive therapy (CDT): The complex decongestive therapy is divided into 2 phases. They are as follows: 1.Volume reduction phase or intensive phase: comprised of manual lymp

Sponsors

Epshita kakati
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Females with unilateral mastectomy for stage I and II breast cancer. 2. Females who have undergone mastectomy 1-3 years prior. 3. Females who have finished treatment i.e chemotherapy, radiotherapy 4. Females diagnosed with breast cancer-associated lymphedema. 5. Female who has undergone breast cancer surgery and experiencing discomfort at the surgical site, swelling in the afflicted limb, and heaviness in the affected limb. 6. Female who has experienced lymphedema with an increase of more than 3 cm compared to the opposite extremity. 7. Ability to walk without assistance at least 100 meters and no contraindications for participating in aerobic exercises.

Exclusion criteria

Exclusion criteria: 1. Females diagnosed with metastatic breast cancer. 2. Female anticipating breast reconstruction within the next six months. 3. Women with any medical conditions that could hinder their ability to engage in exercise, such as decompensated heart failure, unstable ischemic heart disease, severe untreated hypertension, moderate to severe chronic obstructive pulmonary disease, aortic aneurysm, or chronic respiratory insufficiency.

Design outcomes

Primary

MeasureTime frame
Universal Goniometer Hand-held dynamometer Anthropometric measurement using inch tape Micro Respiratory Pressure Meter Timepoint: 4 weeks

Secondary

MeasureTime frame
DASH questionnaire Timepoint: 4 weeks;DASS-21 questionnaireTimepoint: 4 weeks;Harvard Step testTimepoint: 4 weeks;WHOQOL- BREF questionnaireTimepoint: 4 weeks

Countries

India

Contacts

Public ContactEpshita kakati

SGT University

Priyanka.physio@sgtuniversity.org9365004885

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026