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The effect of non-pharmacological relaxation instructions on pain intensity, restlessness and delirium in mechanically ventilated patients after heart surgery

The effect of non-pharmacological relaxation instructions on pain intensity, restlessness and delirium in mechanically ventilated patients after heart surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20130218012509N6
Enrollment
60
Registered
2021-08-13
Start date
2021-07-06
Completion date
Unknown
Last updated
2021-08-30

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

Conditions

Ischemic heart disease. Ischemic heart disease

Interventions

Intervention 1: Intervention group: for the intervention group, a protocol designed including: informing patients by making changes in the environment, music with the content of nature sounds and the

Sponsors

Bagheiat-allah University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Ejection fraction at least 35% Surgery elective Lack of severe drug and alcohol addiction No delirium or impaired level of consciousness before surgery No severe visual or hearing impairment (blindness and deafness) Availability of first-degree family members or causal and relative relatives (at the patient's discretion) who wish to participate in the study

Exclusion criteria

Exclusion criteria: Need for long-term mechanical ventilation as directed by your doctor Need for sedation according to the doctor according to the treatment process Unpredictable events (severe bleeding, severe hemodynamic disturbance, stroke) Death of research units during the study Reluctance and consent of the patient or family to continue participating in the study

Design outcomes

Primary

MeasureTime frame
Pain Intensity. Timepoint: Before and after interventions. Method of measurement: Visual Analogue Scale.;Agitation. Timepoint: Before and after interventions. Method of measurement: Richmond Agitation-Sedation Scale.;Delirium. Timepoint: Before and after interventions. Method of measurement: Confusion Assessment Method for the ICU(CAM-ICU).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactBatul Nehrir

Bagheiat-allah University of Medical Sciences

pirnagmodin1364@yahoo.com+98 21 8755 5576

Outcome results

None listed

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