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effect ear acupressure on pain, anxiety and nausea in patients candidate for appendectomy

The effect of ear acupressure on pain, anxiety and severity of nausea in patients candidated for appendectomy: A three groups randomized clinical trial

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014010416049N1
Enrollment
72
Registered
2014-05-03
Start date
2014-05-05
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Appendicitis. Acute appendicitis, other and unspecified

Interventions

Intervention 1: The intervention group will receive acupressure for 15 minutes in the thalamus point in the ear. Intervention 2: Placebo group will be received acupressure for 15 minutes on adjacent p
Treatment - Other
The intervention group will receive acupressure for 15 minutes in the thalamus point in the ear.
Placebo group will be received acupressure for 15 minutes on adjacent points that are called sham points
In the control group no intervention on patients will be made

Sponsors

chancellor for research, Gonabad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
10 Years to 70 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: 1- Confirmed appendicitis diagnosed by a surgeon 2- The patient is not candidate for emergency appendectomy 3- Patient's consent to participate in this study 4- Without any complications and other medical problems that cause pain, anxiety and nausea 5- Lack of lesion or rash at the site of ear acupressure exercise 6- Consciousness and the ability to report symptoms 7- Not taking pain relief Exclusion criteria: 1- Unwillingness to continue cooperation 2- The clinical condition of the patient that any intervention would be impossible 3- taking pain relief during the intervention period

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Anxiety. Timepoint: Immediately before, after and half an hour after the intervention. Method of measurement: Visual anxiety scale.;Pain. Timepoint: Immediately before, after and half an hour after the intervention. Method of measurement: Visual analog scale.;Severity of nausea. Timepoint: Immediately before, after and half an hour after the intervention. Method of measurement: Measure of visual simulation for nausea.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactArezoo Davarinia Motlagh Ghochan

Gonabad University of Medical Sciences

davarinia.a@gmu.ac.ir; a.davarinia@yahoo.com+98 53 3722 3028

Outcome results

None listed

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