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consumption of iodine during pregnancy

Designing and evaluation of an educational package to provide of adequate iodine status during pregnancy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201602035440N5
Enrollment
100
Registered
2016-02-28
Start date
2014-04-21
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

Iodine status.

Interventions

Intervention 1: Intervention group: the educational program will last four months, and included two face to face educational sessions using a researcher-designed educational pamphlet in the second and
in addition, 2 follows-up by telephone calls will make between educational sessions. urinary iodine concentration (UIC) and salt iodine content will gather at baseline and 4 months after the intervent
Behavior
Intervention group: the educational program will last four months, and included two face to face educational sessions using a researcher-designed educational pamphlet in the second and the third trime
control group: will receive the education usually via health workers provided in health care centers. urinary iodine concentration (UIC) and salt iodine content will gather at baseline and 4 months a

Sponsors

Research institute for endocrine sciences
Lead Sponsor
Research institute for endocrine sciences, Shahid Beheshti University
Collaborator

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Inclusion criteria: Being the first trimester of pregnancy, without thyroid diseases and high blood pressure, willing to cooperate. Exclusion criteria: having any thyroid diseases and hypertension during pregnancy and unwilling to cooperate.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Knowledge. Timepoint: before intervention and 4 months later. Method of measurement: questionnaire.;Attitude. Timepoint: before intervention and 4 months later. Method of measurement: questionnaire.;Practice. Timepoint: before intervention and 4 months later. Method of measurement: questionnaire.;Urinary iodine concentration. Timepoint: before intervention and 4 months later. Method of measurement: acid digestion.;Content of salt iodine. Timepoint: before intervention and 4 months later. Method of measurement: iodometric titration.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactParisa Amiri

Research Center for Social Determinants of Endocrine Health & Obesity Research Center, Research Inst

amiri@endocrine.ac.ir+98 21 2243 2500

Outcome results

None listed

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