Comparing effect of self-hypnosis versus no hypnosis on delivery pain in pregnant women

Comparing effect of self-hypnosis versus no hypnosis on delivery pain in pregnant women: a randomized clinical trial

Status

Recruiting

Phases

Phase 2

Study type

Interventional

Source

IRCT

Registry ID

IRCT20120215009014N199

Enrollment

640

Registered

2017-12-05

Start date

2017-12-06

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

Normal delivery. Term delivery with preterm labor

Interventions

Intervention 1: Intervention group: Normal delivery with self-hypnosis train to pregnant woman during 5 one-hour sessions. Intervention 2: Control group: Normal delivery without hypnosis.

Prevention

Intervention group: Normal delivery with self-hypnosis train to pregnant woman during 5 one-hour sessions

Control group: Normal delivery without hypnosis

Eligibility

Sex/Gender

Female

Age

18 Years to 40 Years

Inclusion criteria

Inclusion criteria: Age of 18 to 40 years Gestational age of 28 months or over

Exclusion criteria

Exclusion criteria: Chronic diseases such as diabetes or cardiovascular diseases Gestational complications such as gestational diabetes or preeclampsia or preterm labor

Design outcomes

Primary

Measure	Time frame
Assessing the severity of pain. Timepoint: During delivery. Method of measurement: Using visual analog scale (VAS).	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammad Rasool Abdoli

Hamedan University of Medical Sciences

mohammad_kola@yahoo.com+98 81 3828 3939

Outcome results

None listed

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