Gestational Diabetes Clinical Trial
— GUIDESOfficial title:
Gestational Diabetes in Uganda and India: Design and Evaluation of Educational Films for Improving Screening and Self-management
Verified date | November 2022 |
Source | London School of Hygiene and Tropical Medicine |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This trial will evaluate a package of three interconnected educational/behavioural interventions aimed at: a) improving knowledge and skills of GDM guidelines and skills of health providers; b) raising awareness of importance of GDM screening among pregnant women and their families; and c) improving confidence and skills in self-management among those diagnosed with GDM. The interventions will be delivered through the medium of film as they are low-cost and scalable, and are particularly suitable for people who are not very literate, making them ideal for low- and middle-income countries (LMICs). The research will be carried out in Uganda (Entebbe) and India (Bengaluru). A careful contextual analysis will precede the development of a culturally-tailored film-based intervention for each setting, which will be iteratively refined using qualitative research methods till it is fit for purpose. The effectiveness of the intervention will be evaluated in independent cluster randomised trials, involving ~10,000 pregnant women across 30 maternity units at each site. The films will be made available in the intervention arm facilities: for viewing by doctors and nurses at their meetings, for continual screening in waiting areas of antenatal clinics, and during group education sessions (and personal mobile use) for GDM patients. Where video/projection facilities are unavailable, small low-cost projectors will be made available. Control arms will follow usual care practices. The principal research question is whether a low-cost educational/behavioural intervention delivered through a package of culturally-tailored films can provide scalable improvements in timely detection and management of GDM. This will be evaluated through assessing three endpoints: a) detection of GDM at 32 weeks of; b) glycaemic control (fasting glucose) in women with GDM at ~34 weeks of pregnancy; and c) adverse perinatal outcomes associated with GDM. Interviews will be conducted with women and health providers to help understand how and why the intervention may be (or may not be) successful. The ultimate aim of the project is to contribute to scientific evidence underpinning the use of films in cost-effectively scaling up behavioural interventions in low literacy settings.
Status | Active, not recruiting |
Enrollment | 16500 |
Est. completion date | May 1, 2023 |
Est. primary completion date | April 1, 2023 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | 18 Years to 50 Years |
Eligibility | Inclusion Criteria: - Pregnant women aged 18 or over attending for antenatal care at participating health facilities. - Pregnant women willing and able to give informed consent. Exclusion Criteria: - Pregnant women <18 years - No informed consent |
Country | Name | City | State |
---|---|---|---|
India | Indian Institute of Public Health | Hyderabad | |
Uganda | MRC/UVRI and LSHTM Uganda Research Unit | Entebbe |
Lead Sponsor | Collaborator |
---|---|
London School of Hygiene and Tropical Medicine | Guy's and St Thomas' NHS Foundation Trust, Indian Institute of Public Health, India, MRC/UVRI & LSHTM Uganda Research Unit |
India, Uganda,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | GDM screening | Proportion of women who were tested for GDM at or after 24 weeks of pregnancy. Self-reported via telephone contact. | 32 weeks of pregnancy | |
Primary | Mean fasting blood sugar (women with GDM) | Mean fasting blood sugar in women diagnosed with GDM. Measured at clinic visit. | 34 weeks of pregnancy | |
Secondary | Adverse perinatal outcomes (composite measure) | Proportion of women with adverse perinatal outcomes related to GDM (composite of emergency caesarean section delivery, perinatal or neonatal mortality, and infant hospitalization within 28 days). Self-reported via telephone contact post delivery. | 28 days postpartum (measured 6 weeks after expected date of delivery (EDD)) |
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