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Enhancing parenting skills for women at risk of perinatal depression in a low-resource setting: a randomised controlled trial of Triple P for Baby

A randomised controlled trial of the effect of a positive parenting Program (Triple P for Baby) on maternal depressive symptoms in pregnant women in a low-resource setting

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12621000073808
Acronym
TPB (Triple P for Baby)
Enrollment
82
Registered
2021-01-29
Start date
2021-03-29
Completion date
2021-08-27
Last updated
2023-01-09

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

Conditions

None listed

Brief summary

The study aims to test the efficacy of a positive parenting program for perinatal depression and infant outcomes. Expectant mothers will participate in a randomised controlled trial. Mothers assigned to the intervention group will engage in 4x2-hour group sessions and 4x30-minute telephone sessions of Triple P for Baby in addition to the care as usual. Mothers assigned to the comparison group will continue with the care as usual for the study duration. In this study, we will collect information regarding participants' mental health, parenting competence, and infants' developmental outcomes at the set assessment points. Differences in depressive symptoms are expected, as well as differences in parenting competence and efficacy that should mediate the type of infant outcomes obtained. We will compare the results on all outcome measures across time and use the data to test the efficacy of the intervention.

Interventions

Study participants will participate in four, 2-hour weekly group sessions of Triple P for Baby (parenting intervention) in the third trimester of pregnancy, followed by four, 30-minute weekly individual telephone sessions delivered postnatally. In total, the intervention will be conducted in eight sessions. Triple P for Baby includes strategies for developing a positive relationship with the baby, teaching the baby new skills and behaviours, responding to the baby, dealing with baby’s crying, pr

Study participants will participate in four, 2-hour weekly group sessions of Triple P for Baby (parenting intervention) in the third trimester of pregnancy, followed by four, 30-minute weekly individual telephone sessions delivered postnatally. In total, the intervention will be conducted in eight sessions. Triple P for Baby includes strategies for developing a positive relationship with the baby, teaching the baby new skills and behaviours, responding to the baby, dealing with baby’s crying, promoting positive sleep habits, dealing with unpleasant emotions, enhancing partner communication, maintaining relationship happiness, and sharing tasks. The program will be delivered by the principal investigator who is an accredited Triple P practitioner/psychologist, and the group sessions will be conducted within the antenatal care clinics at the Moi Teaching and Referral Hospital in Eldoret, Kenya. During the sessions, participants will engage interactively through discussions, group tasks, and role-plays. Participants will be assigned tasks to complete during the session and in-between sessions. Participants will be issued with the Triple P for Baby workbook (Spry, Morawska & Sanders, 2011) describing the session content and homework tasks-including filling in a behaviour monitoring chart and baby diary, which takes about 30 minutes for each day of the 7-day period. The facilitator will use a manual and session checklist to enhance strict adherence to the intervention protocol, and where possible an audio recording of the session will be done for assessment of fidelity. The facilitator manuals have been developed by Triple P International Pty Ltd, Australia and are readily available for purchase and use. The interventionist will receive regular clinical supervision from an accredited Triple P for Baby expert to ensure fidelity in content and program delivery.

Sponsors

The University of Queensland
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Prevention
Masking
Blinded (masking used) (Outcomes Assessor)

Eligibility

Sex/Gender
All
Age
18 Years to 45 Years
Healthy volunteers
No

Inclusion criteria

Participants will be included in the study if they meet the following eligibility criteria: (a) 26 to 32 weeks pregnant, (b) possess high school or equivalent English language competency, (c) at least 18 years of age, (d) living within a radius of 45 minutes’ drive for ease of travel and reach, and (e) screens positive for depressive symptoms.

Exclusion criteria

Participants will be excluded if: a) they cannot read and write English, (b) have a medically reported high-risk pregnancy, (c) are experiencing severe episodes of any form of psychopathology, (d) are currently receiving antidepressant therapy, or (e) currently receiving psychological or counselling services.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026