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A pilot study of a social support intervention for perinatal women.

A social support intervention for perinatal women: A pilot randomized controlled trial of the Bamboo Perinatal Program.

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12625000858493
Enrollment
150
Registered
2025-08-08
Start date
2025-09-01
Completion date
2026-01-31
Last updated
2025-09-08

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

Conditions

None listed

Brief summary

Perinatal depression and anxiety affect 1 in 5 Australian mothers and costs the Australian health care system in excess of $877 million annually. Social support has been consistently shown to (a) assist women in meeting challenges in the postpartum period, (b) reduce postpartum depression, and (c) counteract both postpartum anxiety and stress. The aim of this pilot RCT is to evaluate the feasibility, acceptability, and preliminary effectiveness of an online social support intervention aimed at improving the mental health of first-time mothers.

Interventions

Participants in the intervention (Bamboo) arm will be provided with access to the Bamboo WebApp, where they will indicate whether they prefer to nominate a support person from their existing social network or request for the platform's algorithm to pair them with a volunteer support person (a community-dwelling mother). All support persons will be trained in social support provision via an online training video. The training addresses a variety of principles related to types of social support, t

Participants in the intervention (Bamboo) arm will be provided with access to the Bamboo WebApp, where they will indicate whether they prefer to nominate a support person from their existing social network or request for the platform's algorithm to pair them with a volunteer support person (a community-dwelling mother). All support persons will be trained in social support provision via an online training video. The training addresses a variety of principles related to types of social support, types of coping strategies, rapport building, trust building, autonomy support, active listening, cultural sensitivity, and reinforcement of support boundaries. The training will last approximately 30 minutes. WebApp analytics will capture information on the amount of time each support person spent on the training platform. Support people will check a box to indicate that they have completed the training before progressing in the trial. Once paired, participants and their supporters will be invited to engage in interactive activities on the Bamboo WebApp. These interactive activities include support expectation and planning exercises, discussion topic prompts, and text-based dialogue opportunities. These activities will be non-compulsory, and requirements for frequency and nature of pair-based interactions will not be specified. As such, engagement with the WebApp and volume of support interactions will vary between pairs. Supporters and participants will provide details (volume; nature) of support interactions at assessment times. WebApp analytics will also capture information on engagement with the online materials. Each week, a prompt will be provided on the WebApp to encourage shared planning and support around mental/physical health and parenting. The activities will encourage positive discussions around a range of topics relating to self-care, infant care, and relationships. The WebApp's resource center (containing podcasts, articles and meditations) will be leveraged to identify key principles for healthy and adaptive parenting. These resources will be designed specifically for the trial and program. Participants will have indefinite access to the WebApp. Participants will be eligible to join the trial at any point from the start of their third trimester of pregnancy (28 weeks) through to 1-month postpartum. Pair-matching will take place immediately after allocation to the intervention group, or as soon as possible thereafter. Participation in the trial will continue until 6-months postpartum (i.e., maximum trial duration of approximately 9 months).

Sponsors

James Cook University
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Prevention
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

Participants will be Australian women (a) aged 18years or older, and (b) between the start of their third trimester of pregnancy and 1-month postpartum, and (c) residing in Northern Queensland, Australia. Support people will be either nominated partners/family members/friends or volunteer mothers at least 1-year postpartum, aged 18 years or older. Assigned support people will be female and can be foster or adoptive mothers. Nominated support people can be any gender and are not required to be parents. All support people will reside in Australia.

Exclusion criteria

Exclusion criteria for participants are: (a) women who require more intensive intervention due to current self-reported severe mental health disorder (psychosis, substance use dependence, prescribed anti-psychotic medication) or current overt indicators of family violence (self-reported intervention order; court case for family violence). Exclusion criteria for support people are: (a) people with a self-reported history of criminal activity, and (b) people with self-reported current severe mental health disorder (psychosis, substance use dependence, prescribed anti-psychotic medication).

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026