Effect of family-oriented consultation on nausea and vomiting in primiparous pregnant women

Effect of family-oriented consultation on nausea and vomiting in primiparous pregnant women: a randomized clinical trial

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

IRCT

Registry ID

IRCT201703029014N147

Enrollment

Registered

2017-03-05

Start date

2017-02-19

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

pregnant women. Pregnancy confirmed

Interventions

Intervention 1: Intervention group: Routine care plus family-oriented consultation for 45 min once a week for two weeks. Intervention 2: Control group: Just routine care.

Intervention group: Routine care plus family-oriented consultation for 45 min once a week for two weeks.

Control group: Just routine care.

Eligibility

Sex/Gender

Female

Age

18 Years to 35 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: primiparous pregnant women; age of 18 to 35 years; gestational age of 6 to 8 weeks; mild to moderate gestational nausea and vomiting. Exclusion criteria: Physical or mental disease; using anti-nausea medications.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Assessing nausea and vomiting. Timepoint: before intervention and two weeks after that. Method of measurement: using standard questionnaire PUQE.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFatemeh Khalili

School of Nursing and Midwifery

fa826596@gmail.com+98 81 3838 0572

Outcome results

None listed

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