Skip to content

Effectiveness of Parenting Programs on Child Development and Maternal Well-being in Rural Uganda

Effectiveness of Parenting Programs on Child Development and Maternal Well-being in Rural Uganda

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01906606
Enrollment
360
Registered
2013-07-24
Start date
2013-01-31
Completion date
2014-02-28
Last updated
2016-03-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Child Development, Depression

Keywords

child nutritional status, child development, maternal depression

Brief summary

The purpose of the current study involves the development, implementation and evaluation of a parenting program to target maternal well-being and child health, growth and development in Lira, Uganda. The current study aims to address maternal care within a parenting program as well as parenting practices emphasizing nutrition, hygiene, and psychosocial stimulation through peer-support, practice and problem-solving. Outcomes include child health, growth and development, maternal mental health, mother-child interactions, and maternal-spousal relations. We hypothesize that: 1. Children of parents who attend the parenting program will have better health, height and cognitive/language development at post-test, than children whose parents did not have the opportunity to attend parenting sessions. 2. Parents who attend the parenting program will have more knowledge about child development and provide more home stimulation, dietary diversity and preventive health practices than parents who do not have the opportunity to attend parenting sessions. 3. Mothers who attend the parenting program will have improved well-being compared to mothers who do not have the opportunity to attend parenting sessions.

Interventions

A manualized, community-based 12 session group parenting program, facilitated by a locally recruited volunteer

Sponsors

Mbarara University of Science and Technology
CollaboratorOTHER
McGill University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
12 Months to 36 Months
Healthy volunteers
No

Inclusion criteria

* mothers of children ages 12-24 months

Exclusion criteria

* disabled children

Design outcomes

Primary

MeasureTime frameDescription
Change from baseline in Bayley III Language scaleBaseline and 11 monthsreceptive and expressive language subtests

Secondary

MeasureTime frameDescription
Change from baseline in CES-DBaseline and 11 monthsmaternal depressive symptoms (CES-D) and perceived positive and negative support

Other

MeasureTime frameDescription
Change from Baseline in child length-for-ageBaseline and 11 monthslength for age

Countries

Uganda

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 17, 2026