A clinical trial to study the effect of telecounseling on adherence to the iron tablets and factors of adherence in anemic pregnant women attending antenatal clinic.
Not Applicable
Completed
- Conditions
- Health Condition 1: O280- Abnormal hematological finding onantenatal screening of mother
- Registration Number
- CTRI/2021/09/036603
- Lead Sponsor
- I
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 250
Inclusion Criteria
Anemic pregnant women who are-
�Willing to participate in study.
�Having mobile phone at home.
�In between 13 -16 weeks of gestation.
�Receiving antenatal services.
Exclusion Criteria
�Unavailability of mobile phone in family.
�Withdrawal from the study at any time.
�Known case of Psychiatric Disorder
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Adherence to the IFA supplementationTimepoint: At 4 weeks and 8 weeks.
- Secondary Outcome Measures
Name Time Method Hemoglobin levelTimepoint: 4 weeks and 8 weeks;Predictors of adherence to the IFA supplementationTimepoint: pre-intervention;Satisfaction of telecounsellingTimepoint: 8 weeks