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Tackling Postnatal Depression: Culturally Adapted Learning Through Play Plus (LTP+) Intervention for British Mothers of African and Caribbean Origin

Tackling Postnatal Depression: Culturally Adapted Learning Through Play Plus (LTP+) Intervention for Depressed British Mothers of African and Caribbean Origin

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05148260
Enrollment
80
Registered
2021-12-08
Start date
2023-09-01
Completion date
2026-08-30
Last updated
2022-11-18

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

Conditions

Postnatal Depression

Brief summary

By 2030, depression will be the leading global disease burden. Postnatal depression due to childbirth/parenting leads to long-term negative consequences for mothers, their children and their families. The British African/Caribbean communities are worse hit by the unprecedented impact of post-Covid-19-syndromes, leading to an exponential increase in postnatal depression. Yet, the uptake of mental healthcare by British mothers of African and Caribbean origin is low due to limited access to culturally appropriate care. Theories of attachment and cognitivism were innovatively integrated to examine Learning-Through-Play plus (LTP+) intervention for postnatal depression using a pilot randomised controlled trial. The proposed LTP+ is co-developed and ecologically friendly because it is manualised and can be delivered by non-mental health specialists such as trained community health workers who are more culturally knowledgeable. Findings will be disseminated through academic publications/presentations, policy briefs, original animated videos and podcast series laying the foundations for a psychosocial approach to tackling postnatal depression

Interventions

BEHAVIORALLearning Through Play plus (LTP+)

Group-1: Experimental (n=40 participants) will receive the LTP+ which consist of a total of 12-group integrated treatment sessions lasting approximately 60-90 minutes per session every fortnight with 10 mother/child pair per sub-group.

BEHAVIORALPsychoeducation

Group-2: Controlled (n=40 participants) will receive 'psychoeducation' which consist of a total of 12-group sessions lasting approximately 60-90 minutes per session every fortnight with 10 mother-child pair per sub-group.

Sponsors

Nottingham Trent University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

Only British mothers of African and Caribbean heritage: * experiencing emotional distress due to childbirth or parenting and scored 5 or above on the patient health questionnaire (PHQ-9) * who have children age 0-3 years * residents of designated communities and available for follow-up * are 18 years and above * able to give informed consent.

Exclusion criteria

Are mothers: * with a medical condition that would prevent their participation such as active suicidal ideation, tuberculosis, or heart failure * temporary residents are unlikely to be available for follow up * who are less than 18 years * unable to provide consent. * with non-British African and Caribbean heritage.

Design outcomes

Primary

MeasureTime frameDescription
Change in postnatal depression is being assessedChange is being assessed at baseline, at 12 weeks end of intervention, at 3-months, and at 6-months post-interventionPrimary outcome measure would be assessed using the Patient Health Questionnaire (PHQ-9)
Change in postnatal anxiety is being assessedChange is being assessed at baseline, at 12 weeks end of intervention, at 3-months, and at 6-months post-interventionPrimary outcome measure would be assessed using the Generalised Anxiety Disorder (GAD7) scale
Change in social support is being assessedChange is being assessed at baseline, at 12 weeks end of intervention, at 3-months, and at 6-months post-interventionPrimary outcome measures would be assessed using the Oslo Social Support Scale
Change in health-related quality of life is being assessedChange is being assessed at baseline, at 12 weeks end of intervention, at 3-months, and at 6-months post-interventionOutcome measure would be assessed using the Health-related Quality of Life scale (EuroQoL-5 Dimensions)
Change in service satisfaction is being assessedChange is being assessed at 12 weeks end of interventionOutcome measure would be assessed using the brief Verona Service Satisfaction Scale
Change in child physio-emotional development is being assessedChange is being assessed at baseline, at 12 weeks end of intervention, at 3-months, and at 6-months post-interventionOutcome measure would be assessed using the Ages and Stages Social-Emotional Questionnaire
Change in parenting knowledge of child development is being assessedChange is being assessed at baseline, at 12 weeks end of intervention, at 3-months, and at 6-months post-interventionOutcome measure would be assessed using Learning Through Play Knowledge, Attitude and Practices (KAP) Questionnaire

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026