A trial to study the impact of two educational interventions on the relief of symptoms after operation in breast cancer patients.

Comparative impact of two educational interventions on the shoulder dysfunction, lymphedema and quality of life amongst the breast surgery patients: A Randomized controlled trial

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2012/09/002957

Enrollment

300

Registered

2012-09-04

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- Pre and Post breast surgery patients

Interventions

Intervention1: Self instructional Manual and Video film: Patients undergoing breast surgery will be randomized into three groups: Group I (Preoperative) Group II (Postoperative) Group III (Traditional

Eligibility

Inclusion criteria

Inclusion criteria: Female Biopsy proven breast cancer patients Scheduled to receive breast surgery

Exclusion criteria

Exclusion criteria: Male Any Musculo-skeletal disorder Any physical disability Any mobility problem

Design outcomes

Primary

Measure	Time frame
Percentage of patients developing Shoulder dysfunction. Percentage of patients developing lymphedema. Percentage of patients adhering to nutritional guidelines/diet chartsTimepoint: First follow up at 1 month, then at 3 months and then at 6 months in surgery OPD.	—

Secondary

Measure	Time frame
NillTimepoint: NA	—

Countries

India

Contacts

Public ContactDr Amarjeet Singh

Post Graduate Institute of Medical Education and Research

gsinghpgi@sify.com0172-2756636

Outcome results

None listed

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