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Behavioural Activation (BA) for Postnatal Depression in Blackpool

A Two Phase Pilot of a Behavioural Activation (BA) Programme Specifically Adapted to Support Women Experiencing Postnatal Low Mood in Blackpool

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04183582
Acronym
BA
Enrollment
60
Registered
2019-12-03
Start date
2019-12-31
Completion date
2021-09-30
Last updated
2019-12-03

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

Conditions

Postnatal Depression

Keywords

Psychoeducation, Mental Health, Depression, Postnatal

Brief summary

Is Behavioural Activation feasible, acceptable and potentially effective for mothers experiencing post natal depression in Blackpool? Phase 1: A series of single case studies which aim to examine and refine a) the appropriateness of the programme to women in Blackpool b) the suitability of BA as part of a stepped-care approach to perinatal mental health within the Health Visitor pathway and c) the delivery of the programme in practice. Phase 2: A preliminary single group study examining the quantitative outcomes for participating women (i.e. symptoms of depression, anxiety and general mood, parental stress, responsiveness, and behavioural avoidance and activation.

Interventions

Behavioural Activation is a treatment for depression, the current programme has been adapted to suit the needs of postnatal women Session 1: Getting Started Session 2: Identifying Triggers, Reactions and Avoidance Patterns (TRAPs) Session 3: Turning TRACs in to Triggers, Reactions and Alternative Coping (TRACs) Session 4: Support and Communication Session 5: Being a Good Enough Mum Session 6: Staying Well

Sponsors

National Society for the Prevention of Cruelty to Children
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Masking description

No masking

Intervention model description

Experimental Arm - single group study

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 50 Years
Healthy volunteers
No

Inclusion criteria

* 18 years or older * Score between 10-19 on PhQ9 * Have given birth within the last 6 months * Willing to engage in a psychological therapy * Informed, prepared and safe to participate in the programme * Able to understand spoken and basic written English

Exclusion criteria

* Under 18 years old * Score under 10 or over 19 on the PHQ9 * Receiving another from of psychological treatment for depression * Unwilling to engage in a psychological therapy * Another primary area of difficulty which takes precedence over the current programme (e.g.substance dependency disorders, suicidal crises, frequent, serious and deliberate self-harm, acute threat in the form of serious interpersonal violence from a partner or friend or family member, and evidence of more serious mental health disorders which may require additional support, i.e., psychotic disorders, Bipolar Disorder

Design outcomes

Primary

MeasureTime frameDescription
Snaith-Hamilton Pleasure Scale (SHAPS)Baseline and 6 weeksThe SHAPS is a 14-item measure of anhedonia (the degree to which an individual is able to experience pleasure). It comprises of four subscales which measure response/hedonic experiences; interests/past-times, social interaction, sensory experiences, food/drink.
Parental Stress Scale (PSS)Baseline and 6 weeksThe PSS is a self-report scale that intended to assess parental stress. It contains 18 items representing pleasure or positive themes of parenthood (emotional benefits, self-enrichment, personal development) and negative components (demands on resources, opportunity costs and restrictions).
Maternal Infant Responsiveness Instrument (MIRI)Baseline and 6 weeksThe MIRI is a 22-item scale designed to measure the parent's feelings about the infant and an appraisal of their infant's responsiveness.
Behavioural Activation for DEpression Scale (BADS)Baseline and 6 weeksThe BADS is a 25-item scale which can track change in behaviours which are hypothesised to underlie depression which are specifically targeted through Behavioural Activation. It comprises of four subscales; activation, avoidance/rumination, work/school impairment and social impairment.
Patient Health Questionnaire (PHQ9)Baseline, 6 weeks, 18 weeks, 1 yearThe PHQ9 is a 9-item multi-purpose instrument which can be used to screen, diagnose, monitor and assess symptoms of depression.
Generalised Anxiety Disorder Questionnaire (GAD7)Baseline and 6 weeksThe GAD7 is a 7-item multi-purpose instrument which can be used to screen, diagnose, monitor and assess symptoms of anxiety.

Secondary

MeasureTime frameDescription
Ages and Stages Questionnaire (ASQ)Data collected when child is 1 year and 2-2.5yearsNationally mandated data collected by Health Visitors in the UK to assess children's development. This includes five key areas of development, communication, gross motor, fine motor, problem solving, and personal-social.

Other

MeasureTime frameDescription
Edinburgh Postnatal Depression Scale (EPDS)Baseline, 2 week (x2), 3 weeks (x2), 4 weeks, 5 weeks, 6 weeksThe EPDS is a 10-item measure which assesses low mood and symptoms of depression. It has been designed specifically for women in the postnatal period.

Countries

United Kingdom

Contacts

Primary ContactMiss E Lowrie, PhD
Emma.CECD@nspcc.org.uk01253 476611
Backup ContactMrs C Law, MSc
Clare.CECD@nspcc.org.uk01253 476192

Outcome results

None listed

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