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The effect of acupressure in patients on a ventilator

Evaluation of the effect of acupressure on pain, restlessness and sedation in ventilator patients

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20220626055279N1
Enrollment
60
Registered
2022-07-18
Start date
2022-07-23
Completion date
Unknown
Last updated
2022-08-29

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

Conditions

Patients with reduced level of consciousness in the intensive care unit.

Interventions

Intervention 1: Intervention group: Acupressure is performed using a special bracelet in the lower wrist area (Nigoan area or P6) of both hands for 5 minutes at the same time. This procedure is perfor

Sponsors

Arak University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Anesthetized patients hospitalized in the intensive care unit who have been treated with mechanical ventilation (SIMV, PSV, CPAP, BIPAP) for 24 hours before and during the intervention. Age of 18-65 years old. Stable hemodynamic status of patients. GCS score 7 and above. Not having a wound or any lesion in the desired area for acupressure. Not having a history of mental illness and not taking psychiatric drugs according to the patient's companion. Absence of cardiovascular diseases Having a prescription for a sedative.

Exclusion criteria

Exclusion criteria: Death or transfer of the patient from the intensive care unit. Separation from mechanical ventilation. Decreased level of consciousness to less than 7. Induction of anesthesia and use of drugs with neuromuscular blocking effect. A sudden change in the patient's clinical condition due to cardiopulmonary arrest, severe bleeding and other conditions that require medical interventions or surgery. The interference of the bracelet used to physically restrain the patient with the area used in acupressure.

Design outcomes

Primary

MeasureTime frame
Pain score. Timepoint: Pain assessment is done during the study (3 days), and twice everyday at 12-13 and 18-19. Method of measurement: Pain score is measured using Behavioral Pain Scale (BPS).;The score of calmness and restlessness. Timepoint: During the study (3 days), and twice everyday at 12-13 and 18-19. Method of measurement: Using the Richmond scale.;The amount of used sedatives. Timepoint: End of the study period. Method of measurement: Report the amount of medicine taken for the patient in the patient's file.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactKorosh Rezaei

Arak University of Medical Sciences

rezaeikorosh0@gmail.com+98 86 3417 3463

Outcome results

None listed

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