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A study to evaluate the effectiveness of exercise protocol in decreasing pain,numbness and swelling in arm,improving range of motion and strength in arm and improving quality of life among women with breast cancer who have undergone breast surgery.

A study to assess the effectiveness of exercise protocol on upper arm dysfunction and quality of life among women with breast cancer who have undergone mastectomy with axillary lymph node dissection.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2016/04/006897
Enrollment
44
Registered
2016-04-29
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- Upper arm dysfunction and quality of life among women with breast cancer who have undergone mastectomy with axillary lymph node dissection.

Interventions

Intervention1: Exercise protocol (exercises to decrease upper arm dysfunction) : Exercise till 1 week after surgery,exercises from 2nd to 8th week after surgery Control Intervention1: Normal post mast

Sponsors

Dr Anurag Srivastava
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Women diagnosed with unilateral Breast cancer admitted in surgical ward and BRAIRCH oncology ward , AIIMS and are scheduled for mastectomy with axillary lymph node dissection. Patients who are able to follow instructions. Patients who have given consent for participation in the study. Able to communicate in Hindi /English .

Exclusion criteria

Exclusion criteria: Patients not willing to participate in the study. Patients who have major health problems or disabilities like gross obesity (BMI >35 ), Cardiovascular diseases (angina , MI within last 6 months). Patients having primary lymphedema and any contraindication to the affected upper-limb exercises(e.g., venous thrombosis).. Patients who are not able to follow instructions. Patients who have cognitive dysfunction .

Design outcomes

Primary

MeasureTime frame
Upper arm dysfunction assessed by Disability of Arm Shoulder and Hand Questionnaire (DASH) score from pretest to postestTimepoint: 3 time points,1 pretest and 2 posttest

Secondary

MeasureTime frame
Quality of life assessed by European organization for research and treatment of cancer quality of life questionnaire (EORTC QLQ-C30)and Breast module(EORTC-QLQ-BR23)Timepoint: 3 time points,1 pretest and 2 posttest

Countries

India

Contacts

Public ContactDr Anurag Srivastava

All India Institute of Medical Sciences,New Delhi

gaddamrachel@gmail.com9953224917

Outcome results

None listed

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