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Comparing the effect of auricular acupressure and body acupressure on pain and anxiety

Comparing the effect of auricular acupressure and body acupressure on pain and anxiety in older adults undergoing knee replacement arthroplasty

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20110912007529N28
Enrollment
141
Registered
2023-07-10
Start date
2023-08-23
Completion date
Unknown
Last updated
2024-03-06

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

Conditions

Knee joint replacement.

Interventions

Intervention 1: Intervention group: interventional therapy ear acupuncture At first, disinfection of both outer auricles using 70% alcohol, and then during 3 days, every day three times, each time for

Sponsors

Shahed University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
60 Years to No maximum

Inclusion criteria

Inclusion criteria: Age 60 years and over Absence of cognitive impairment Ability to communicate Non-alcohol and drug addiction Lack of experience or simultaneous participation in similar training sessions Lake of history of mental illness The first experience with knee replacement arthroplasty Undergoing spinal anesthesia Lake of malignancy, lake of inflammatory disease, and vascular disease Having no active bleeding, sensory disorders, pain, infectious wounds and skin disease at the intervention site

Exclusion criteria

Exclusion criteria: Unwillingness to co-operate with a patient or physician Return to the operating room

Design outcomes

Primary

MeasureTime frame
Intensity of pain. Timepoint: Before the first intervention on the first day, after the last intervention on the first day, after the last intervention on the second day, and after the last intervention end on the third day. Method of measurement: Visual Pain Scale.;Quality of pain. Timepoint: Before the first intervention on the first day, after the last intervention on the first day, after the last intervention on the second day, and after the last intervention end on the third day. Method of measurement: MacGill questionnaire.;Intensity of anxiety. Timepoint: Before the first intervention on the first day, after the last intervention on the first day, after the last intervention on the second day, and after the last intervention end on the third day. Method of measurement: Visual Analogue Scale Anxiety) VASA).;Quality of anxiety. Timepoint: Before the first intervention on the first day, after the last intervention on the first day, after the last intervention on the second day, and after the last intervention end on the third day. Method of measurement: The Spielberger Inventory.

Secondary

MeasureTime frame
Blood pressure. Timepoint: Before the first intervention on the first day, after the last intervention on the first day, after the last intervention on the second day, and after the last intervention end on the third day. Method of measurement: Digital arm l sphygmomanometer.;Pulse rate. Timepoint: Before the first intervention on the first day, after the last intervention on the first day, after the last intervention on the second day, and after the last intervention end on the third day. Method of measurement: Enumeration of pulse rate.;Respiration rate. Timepoint: Before the first intervention on the first day, after the last intervention on the first day, after the last intervention on the second day, and after the last intervention end on the third day. Method of measurement: Enumeration of Respiration rate.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Nahid Rejeh

Shahed University

nrejeh@yahoo.com+98 21 5121 2100

Outcome results

None listed

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