Impact of Behavioural Modification Working Toolkit Among Women With Gestational Diabetes Mellitus and Hypertension
Recruiting · NCT07551011 · Interventional (participants receive a specific treatment) · Lead sponsor: University of the Punjab
View the official record on ClinicalTrials.gov →Interventions studied
Behavioral Modification Working (BMW) ToolkitRoutine Antenatal Care
What this trial is about
This trial aims to evaluate the effectiveness of a Behavioral Modification Working (BMW) Toolkit in improving glycemic control and blood pressure among pregnant women diagnosed with both GDM and PIH.
Who can take part
Age range
15 Years to 49 Years
Sex
Female
Healthy volunteers
No - a diagnosis or condition is required
Phase
Not applicable (e.g. observational or device study)
Study type
Interventional (participants receive a specific treatment)
Inclusion criteria
- Pregnant women aged 15-49 years.
- Gestational age between 16 and 20 weeks at enrolment.
- Diagnosed with both gestational diabetes mellitus (GDM) and pregnancy-induced hypertension (PIH).
- At least one prior antenatal visit at the study site.
Exclusion criteria
- Pre-existing diabetes mellitus or chronic hypertension prior to pregnancy.
- Pre-existing renal disease, thyroid disease, or major hematological disorders.
- Multiple pregnancy (e.g., twins, triplets).
- Severe psychiatric illness.
Where it is running
2 locations listed.
- Shaikh Zayed Hospital - Lahore, Punjab Province, Pakistan
- Sir Ganga Ram Hospital - Lahore, Punjab Province, Pakistan