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The evaluation of effect of acupressure on primary dysmenorrheal

The evaluation of effect of acupressure on primary dysmenorrheal

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT138808272731N1
Enrollment
200
Registered
2010-02-16
Start date
2008-10-22
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

primary dysmenorrhea. Pain and other conditions associated with female genital organs and menstrual cycle

Interventions

Intervention 1: In the experiment group, acupressure done on liv3 point located two thumb-widths behind the skin-margin between the first (big) and second toes for 3-7 days before the onset of menstru
In the experiment group, acupressure done on liv3 point located two thumb-widths behind the skin-margin between the first (big) and second toes for 3-7 days before the onset of menstruation for 20 min
In the control group, acupressure done on placebo point located two thumb-widths behind the skin-margin between the first (big) and second toes for 3-7 days before the onset of menstruation for 20 min

Sponsors

Tarbait Modares University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 21 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: age 18-21 years, having regular menstrual cycles (duration of 3-8 days and interval of 21-35 days). presence of moderate to severe pain i.e. a score of 4 or more on a wrong-Baker faces pain scale, presence of symptoms of liver channel, presence of fix or sharp pain in lower abdomen for 1-2 day prior to onset of menstruation, distension feel in abdomen and breast, presence of dark-colored menstruation with clotting, irritability or depression and sometimes sleeplessness prior to onset of menstruation, tongue with red-colored seed, worsening the pain with pressure on abdominal), no prior history of gynecological disease or abdominal or pelvic surgery, no pain during menstrual cycle or menstruation duration, 2 hours after meal Exclusion criteria: history of mental stress in last 6 month especially having moderate to severe level of depression (score of 19 or more in beck-21 inventory), taking analgesics during 4 hours before intervention, menstruation cycle lower than 25 days or more than 35 days, use of tobacco products, or alcohol, presence of verbal, audible, mental problems, heart disease, kidney disease, diabetes mellitus, asthma, hyperthyroid or hypothyroid, or respiratory disease, presence of scar or inflammatory disease in acupoint.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Liver channel symptoms. Timepoint: first and fourth cycles. Method of measurement: liver channel symptoms questionnare-interview to patient.;Severity of dysmenorrhea. Timepoint: first and fourth cycles. Method of measurement: multidimensional scoring system -interview with patient.;Pain severity. Timepoint: monthly. Method of measurement: wrong-Baker faces pain scale-interview to patient.;Pain duration. Timepoint: monthly. Method of measurement: questionnare-interview to patient.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFatemeh Bazarganipour

Tarbiat Modares University

fatimabazargani@yahoo.comf.bazarganipour@gmail.combazarganipour@modares.ac.ir+98 2188220209396

Outcome results

None listed

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