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The impact of cardio-oncology rehabilitation in breast cancer patients

The impact of cardio-oncology rehabilitation on dyspnea, fatigue, lymphedema and quality of life in breast cancer patients receiving chemo-radiotherapy - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/12/078322
Enrollment
32
Registered
2024-12-19
Start date
Unknown
Completion date
Unknown
Last updated
2025-02-03

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: Group 1- Expiratory Muscle Training with Conventional Chest physiotherapy with kinesio taping and relaxation exercises: PEP IMT sessions per day, consisting of 30 breaths against a resi

Sponsors

Aaliya Javed
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1) Female breast cancer patients diagnosed with Stage I-III. 2) Stable patients with breast cancer who have completed the adjuvant treatment or were allowed to undergo the treatment. 3) Willingness to participate in cardio-oncology rehabilitation sessions. 4) Ability to comprehend and respond to questionnaires or assessments related to dyspnea, fatigue, lymphedema, and quality of life. 5) Ability to provide informed consent for participation in the study.

Exclusion criteria

Exclusion criteria: 1) Presence of uncontrolled cardiac symptoms. 2) Patients with metastatic breast cancer or Stage IV disease. 3) History of significant cardiovascular diseases or conditions that contraindicate participation in cardio-oncology rehabilitation. 4) Severe psychiatric disorders that may impede participation in the study or comprehension of study procedures. 5) Pregnancy, as it may affect the interpretation of study outcomes and participation in rehabilitation exercises.

Design outcomes

Primary

MeasureTime frame
1) Modified Borg Scale 2) Respiratory muscle functionTimepoint: 4 weeks

Secondary

MeasureTime frame
1) Arm circumference 2) EORTC QLQ-C30 questionnaire 3) NPRS 4) Brief Fatigue Inventory/Modified Brief Fatigue InventoryTimepoint: 4 weeks

Countries

India

Contacts

Public ContactAaliya Javed

SGT University

neha_fphy@sgtuniversity.org8826043916

Outcome results

None listed

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