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The Effect of Acupressure on Abortion

The Investigation of the effect of acupressure on pain intensity and anxiety in hospitalized women in Niknafs maternity hospital in Rafsanjan, 2020

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20210310050657N1
Enrollment
120
Registered
2021-12-01
Start date
2021-11-21
Completion date
Unknown
Last updated
2022-01-11

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

Conditions

Abortion. Missed abortion

Interventions

Intervention 1: Intervention group: Acupressure at LI4 point (in middle of the angle between the first and second bones of the palm between the thumb and index finger on the back of the hand) bilatera

Sponsors

Rafsanjan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: Women aged 18 to 45 years Hospitalization with a diagnosis of spontaneous or induced abortion Having a pain score higher than 3 based on the VAS scale Single pregnancy Gestational age less than 20 weeks based on LMP or ultrasound No lesions at the site of acupressure Having enough cognitive power to answer research questions No drug and alcohol abuse No history of known mental illness

Exclusion criteria

Exclusion criteria: Cases of severe bleeding at admission Taking any sedative before entering the study septic abortion cases

Design outcomes

Primary

MeasureTime frame
Pain during abortion. Timepoint: Measurement of previous pain, immediately after and 30 minutes after the intervention. Method of measurement: The data collection tool will consist of three parts. The first part contains the demographic information questionnaire, the second part contains the 10-point visual instrument for measuring pain (VAS). The third part includes the Spielberger Anxiety Standard Questionnaire.

Secondary

MeasureTime frame
Anxiety. Timepoint: Before the commence of intervention, immediately after the intervention and 30 minutes after the finishing of intervention. Method of measurement: Spielberger Anxiety Standard Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactZohreh Sahebi Sham Abadi

Rafsanjan University of Medical Sciences

sahebizm@rums.ac.ir+98 34 3423 0559

Outcome results

None listed

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