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The study of the effect of acupressure on Hugo point on delivery pain of multiparous women

The study of the Effect of acupressure on Hugo point on delivery pain of multiparous women

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016112321670N2
Enrollment
62
Registered
2017-01-31
Start date
2017-01-19
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

The relationship of acupressure on Hugo point and delivery pain. False labour at or after 37 completed weeks of gestation

Interventions

Intervention 1: Intervention group: For this group, Hugo point will be pressured by researcher for 4 cycles. Each pressure course will take 20 minutes in which, first the Hugo point will be pressured
Intervention group: For this group, Hugo point will be pressured by researcher for 4 cycles. Each pressure course will take 20 minutes in which, first the Hugo point will be pressured lightly and the
Control group: In this group, an irrelevant point other than Hugo point will be pressured by researcher for 4 cycles. Each pressure course will take 20 minutes in which, first the Hugo point will be p

Sponsors

Abadan 17 Shahrivar hospital
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Inclusion criteria: Vaginal delivery; second to fourth pregnancy; gestational age between 37 to 42 weeks; complaint of moderate to severe delivery pain based on the standard visual pain scale assessment; infant birth weight between 2500 to 4000 gram; body mass index between 18.5 to 29 Exclusion criteria: Hard and prolonged delivery; addiction; history of cesarean section and intra-abdominal surgery; history of postpartum hemorrhage

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
The primary outcome measure of this study is severity of delivery pain. Timepoint: The severity of delivery pain will be assessed before and after each pressure course. Method of measurement: Severity of delivery pain will be assessed using standard visual pain scale assessment.

Secondary

MeasureTime frame
Secondary outcome measure of this study is the duration of delivery pain. Timepoint: Duration of delivery pain will be assessed before and after of each pressure course. Method of measurement: Duration of delivery pain will be asked from participants and recorded.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactShahla Afravi

Abadan 17 Shahrivar hospital

af.shahla@yahoo.com+98 61 5335 4546

Outcome results

None listed

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