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Health education for the prevention of secondhand smoke exposure among pregnant women visiting the antenatal clinic at a university hospital

The effectiveness of health education for the prevention of secondhand smoke exposure among pregnant women visiting the antenatal clinic at a university hospital: a randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN32178828
Enrollment
100
Registered
2016-04-11
Start date
2016-03-01
Completion date
Unknown
Last updated
2016-10-17

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

Conditions

Secondhand smoke exposure in pregnant women Pregnancy and Childbirth

Interventions

Face-to face counseling (one session which takes 15-20 minutes) and written information (leaflet) compared to only written information about health risks of exposure to secondhand smoke for pregnant

Sponsors

King Saud University, Deanship of Scientific Research
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1. Arabic speaking pregnant non –smoker women 2. <25 weeks of pregnancy to give time for the intervention (1 month) and the follow up 3. Living with smoking person (husband, brother, father, son, father- in- low, house helper or other) 4. Literate 5. Willing to participate in the study

Exclusion criteria

Exclusion criteria: Women with unknown smoking status

Design outcomes

Primary

MeasureTime frame
1. Reduction in time of pregnant woman exposure to secondhand smoke 2. Increased knowledge about health risks of exposure to secondhand smoke on the pregnant woman and her unborn child 3. Improvement of behavior of avoidance of secondhand smoke exposure by pregnant women All outcomes will be measured using pre/post intervention validated questionnaire. The outcomes will be measured 4 weeks after interventions.

Secondary

MeasureTime frame
1. Rate of quitting of person/persons smoking in the presence of the pregnant woman 2. All outcomes will be measured using pre/post intervention validated questionnaire The outcomes will be measured 4 weeks after interventions.

Countries

Saudi Arabia

Outcome results

None listed

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