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The success of improving the overall quality of life using less restricted chest bone movements over restricted chest bone movements in individuals undergoing open heart surgery.

The effectiveness of modified sternal precautions vs standard sternal precautions in patients undergoing cardiac surgery via median sternotomy an experimental study - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/09/074227
Enrollment
118
Registered
2024-09-24
Start date
Unknown
Completion date
Unknown
Last updated
2024-10-14

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

Conditions

Health Condition 1: I251- Atherosclerotic heart disease of native coronary artery

Interventions

Intervention1: Modified Sternal Precautions for patients undergoing cardiac surgery via median sternotomy: 1. Use pain and discomfort to guide the safe use of the arms
2. Avoid pushing or pulling with one arm
3. Use both arms close to the body during lifting
4. Use of arms is possible, but keep them close to the body
5. Avoid stretching one or both arms backwards at the same time
6. Use a cushion or perform sternal preservation technique (crossing the arms in a ‘self-hugging’ posture) when coughing
7.When transferring, roll onto the side, ease the legs over the edge of the bed and carefully use the arms to sit up from a lying position For a period of 3 weeks Control Intervention1: Standard St
2. Avoid one-arm (unilateral) activity
3. Limit the elevation of the arms to 90 degrees
4. Avoid lifting objects heavier than 2 kg
5. Avoid placing the arms behind the back For 3 weeks

Sponsors

NIL
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1) Age – 18 years to 60 years 2) Gender – both 3) Conscious and oriented 4) All adults who have undergone cardiac surgery involving a median sternotomy. 5) Able to provide informed consent.

Exclusion criteria

Exclusion criteria: 1) Unable to understand verbal instructions in English 2) Age less than 18 years 3) Burns or any other skin diseases 4) Patients on invasive ventilator support

Design outcomes

Primary

MeasureTime frame
36 Item Short Form Survey (SF-36)Timepoint: The questionnaire will be administered at the end of 3 weeks over a telephonic interview

Secondary

MeasureTime frame
Short Form McGill Pain Questionnaire 2 (SF-MPQ-2)Timepoint: The questionnaire will be administered at the end of 3 weeks over a telephonic interview

Countries

India

Contacts

Public ContactShraddha A Bhargav

Narayana Hrudayalaya Institute of Physiotherapy

ndjk2011@gmail.com9791644870

Outcome results

None listed

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