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Effects of pre operative education program on comfort, anxiety and patient ventilator synchrony among post CTVS surgery patients.

A randomized control trial to assess the effects of a preoperative education program on comfort, anxiety and patient ventilator synchrony among post CTVS surgery patients admitted in the CTVS department at AIIMS, New Delhi. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/04/108305
Enrollment
80
Registered
2026-04-13
Start date
Unknown
Completion date
Unknown
Last updated
2026-04-27

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 Health Condition 2: I35- Nonrheumatic aortic valve disorders Health Condition 3: I34- Nonrheumatic mitral valve disorders Health Condition 4: I06- Rheumatic aortic valve diseases Health Condition 5: I05- Rheumatic mitral valve diseases

Interventions

Intervention1: Preoperative education program: Preoperative education begins with welcoming the patient, introducing oneself, and explaining the purpose of the session, which is to prepare the patient

Sponsors

Shagun Singh
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients having Age 18-60 years 2. Scheduled for elective cardiac surgery (CABG, valve replacement or repair, combined procedures) 3. Expected to require postoperative mechanical ventilation 4. Ability to understand and communicate in Hindi or English 5. Conscious and oriented (Glasgow Coma Scale score equal to 15) 6. Willingness to participate in the study

Exclusion criteria

Exclusion criteria: 1. Age less than 18 or more than 60 2. Emergency or urgent cardiac surgery 3. Documented psychiatric disorders or currently on psychiatric medications 4. Severe cognitive impairment or diagnosed dementia 5. Hearing or visual impairments that preclude participation in education 6. Previous cardiac surgery (redo procedures) 7. Severe preoperative hemodynamic instability requiring inotropic support or intra-aortic balloon pump 8. Illiterate with no family member available to assist 9. Participation in another interventional research study 10. Preoperative mechanical ventilation 11. History of smoking, COPD or other severe comorbidities

Design outcomes

Primary

MeasureTime frame
comfort, anxiety and patient ventilator synchronyTimepoint: 30 mins after waking up from sedation, 30 mins after extubation—

Secondary

MeasureTime frame
compare the duration of mechanical ventilation between intervention group & control groupTimepoint: baseline—

Countries

India

Contacts

Public ContactShagun Singh

AIIMS, New Delhi

smitadas307@gmail.com9871755975

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: May 1, 2026