Mental Health, Gender-Based Violence, and Stunting in Tanzania
NCT ID: NCT06065293
Last Updated: 2023-10-10
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
162 participants
OBSERVATIONAL
2023-01-01
2023-09-07
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
This study is a secondary data analysis of de-identified survey and stunting data that were conducted as a part of a needs assessment by a local nonprofit organization in Tanzania. The needs assessment was conducted to inform a mental health initiative organized by the established nonprofit across 5 villages in rural Tanzania. This project's primary aims are:
* To determine the prevalence of mental health and family relationship problems in five villages
* To determine associations between intimate partner violence (IPV) mental health and substance use and childhood stunting
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Impact of Maternal Stress on Infant Stunting
NCT02755012
Engaging Fathers for Effective Child Nutrition and Development in Tanzania
NCT03759821
Achieving Sustained Early Child Development Impacts at Scale: A Test in Kenya
NCT06140017
Essential Coaching for Every Mother in Tanzania
NCT05362305
Evaluation of Scaling Up Early Childhood Development in Zambia
NCT03991182
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
OTHER
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Mothers involved in a local non-profit
No interventions assigned to this group
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* participating in a local nonprofit
* pregnant or having a child under 2 years old
Exclusion Criteria
* Not participating in the local nonprofit
* Not pregnant or having a child under 2 years old
FEMALE
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Colorado State University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Shelley Haddock, PhD
Role: PRINCIPAL_INVESTIGATOR
Colorado State University
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Colorado State University
Fort Collins, Colorado, United States
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
3916
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.