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Mindfulness-based Intervention for Postnatal Depression

The Impacts of Mindfulness-based Intervention on Symptoms and Cognition in Chinese Women With Postnatal Depressive Symptoms - A Randomized Controlled Clinical Trial

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04332146
Enrollment
70
Registered
2020-04-02
Start date
2017-11-01
Completion date
2020-05-31
Last updated
2026-01-27

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

Conditions

Postnatal Depression

Brief summary

Postnatal psychopathology have adverse impact on both mothers and infants. Few postnatal women with depressive symptoms receive treatment, and pharmacological intervention has not been well accepted due to the medication side-effects. Recently, mindfulness-based interventions were found to be beneficial for symptoms in perinatal and antenatal women with depression. These non-pharmacological interventions require less resources and are more feasible for postnatal women to practice at home. To date, no randomized controlled trial has examined mindfulness-based intervention program as a treatment for women with postnatal depression. The proposed randomized controlled trial aims to examine the effects of an 8-week mindfulness-based intervention program on symptom and cognition for postnatal females with depressive symptoms. A total of 70 postnatal women with depressive symptoms will be recruited from the psychiatric outpatient clinics in Hong Kong, and will be randomized into two groups: 1) an 8-week mindfulness-based intervention program (n=35); 2) a booklet-based psychoeducation control group (n=35). All participants will be assessed for depression, anxiety, stress, cognition, role functioning, quality of life, sleep quality and mindfulness ability at the baseline, 8 weeks, and 3 months after intervention. The intervention sessions will be held once weekly lasting 90 minutes for 8 weeks. The investigators primarily hypothesize that participants in the mindfulness-based intervention group will improve depressive symptom after 8 weeks compared with the control group. Secondary, the mindfulness-based intervention will improve anxiety, stress, cognitive functions, sleep quality, quality of life and mindfulness ability.

Interventions

BEHAVIORALMindfulness-based program (MBI-p-R)

The MBI-p-R was developed in line with the model of Mindfulness-based Stress Reducation (MBSR) proposed by Kabat-Zinn. It will be conducted for 1.5 hours for each session, once a week for 8 weeks. There are four key operational components to be included in each session: engagement and introduction, mindfulness practices, daily life application, and consolidation of learning.

BEHAVIORALBooklet-based psychoeducation

The participants in the control group will be provided a booklet at baseline, including general information in handling every day stress by a new mother, as well as a record for their weekly activities. The contents covered a range of topics including work-stress, balanced diet, physical exercise, sleeping quality, bonding with baby and the treatment for depression. The participants will be contacted by phone call and/or whatsapp weekly for a short talk based on the record and content on the booklet. They will also be asked to record their daily life weekly for discussion.

Sponsors

The University of Hong Kong
Lead SponsorOTHER

Study design

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

Eligibility

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

Inclusion criteria

* Females aged from 18 and above * The Edinburgh Postnatal Depression Scale cut-off score of \>=9 * At least 6 weeks, and up to one and half years after childbirth * Cantonese-speaking Chinese

Exclusion criteria

* Severe physical illness (myocardial infarction, hypertension, fracture, spinal problems in which yoga may be contraindicated), and seizure disorders. * Comorbid substance dependence * Women with psychotic depression, severe eating disorders, actively suicidal or obsessive-compulsive disorders * Known pregnancy * A history of bipolar disorder, schizophrenia, brain trauma or organic brain disease, mental retardation, or antisocial personality disorder * Practice of mindfulness (in forms of Tai Chi, Qi gong or yoga etc.) more than twice a week during the previous three months.

Design outcomes

Primary

MeasureTime frameDescription
Change from Baseline Depression at 8 weeksChange from baseline to 8 weeksThe Edinburgh Postnatal Depression Scale, total score 0-30, higher scores mean worse outcome.
Change from 8 weeks Depression at 3 monthsChange from 8 weeks to 3 monthsThe Edinburgh Postnatal Depression Scale, total score 0-30, higher scores mean worse outcome.

Secondary

MeasureTime frameDescription
Change from Baseline Role Functioning at 8 weeksChange from baseline to 8 weeksRole Functioning Scale, minimum 4, maximum 38, higher scores mean better outcome.
Change from 8 weeks Role Functioning at 3 monthsChange from 8 weeks to 3 monthsRole Functioning Scale, minimum 4, maximum 38, higher scores mean better outcome.
Change from Baseline Anxiety at 8 weeksChange from baseline to 8 weeksDepression Anxiety Stress Scale, Anxiety subscore 0-42, higher scores mean worse outcome.
Change from 8 weeks Anxiety at 3 monthsChange from 8 weeks to 3 monthsDepression Anxiety Stress Scale, Anxiety subscore 0-42, higher scores mean worse outcome.
Change from Baseline Stress at 8 weeksChange from baseline to 8 weeksDepression Anxiety Stress Scale, Stress subscore 0-42, higher scores mean worse outcome.
Change from 8 weeks Stress at 3 monthsChange from 8 weeks to 3 monthsDepression Anxiety Stress Scale, Stress subscore 0-42, higher scores mean worse outcome.
Change from Baseline Executive Function at 8 weeksChange from baseline to 8 weeksTrial Making Test, reaction time is recorded, shorter time means better outcome.
Change from 8 weeks Executive Function at 3 monthsChange from 8 weeks to 3 monthsTrial Making Test, reaction time is recorded, shorter time means better outcome.
Change from Baseline Attention at 8 weeksChange from baseline to 8 weeksLetter Cancellation Test, correct rate and time are recorded, higher correct rate and shorter time mean better outcome.
Change from 8 weeks Attention at 3 monthsChange from 8 weeks to 3 monthsLetter Cancellation Test, correct rate and time are recorded, higher correct rate and shorter time mean better outcome.
Change from Baseline Working Memory at 8 weeksChange from baseline to 8 weeksDigit-Span Test, minimum 0, maximum 14, higher scores mean better outcome.
Change from 8 weeks Working Memory at 3 monthsChange from 8 weeks to 3 monthsDigit-Span Test, minimum 0, maximum 14, higher scores mean better outcome.
Change from Baseline Quality of Life at 8 weeksChange from baseline to 8 weeksThe Short Form Health Survey, minimum score 0, and maximum score 100, higher scores mean better outcome.
Change from 8 weeks Quality of Life at 3 monthsChange from 8 weeks to 3 monthsThe Short Form Health Survey, minimum score 0, and maximum score 100, higher scores mean better outcome.
Change from Baseline Sleep Quality at 8 weeksChange from baseline to 8 weeksPittsburg Sleep Quality Index, minimum 0, maximum 21, higher scores mean worse outcome.
Change from 8 weeks Sleep Quality at 3 monthsChange from 8 weeks to 3 monthsPittsburg Sleep Quality Index, minimum 0, maximum 21, higher scores mean worse outcome.
Change from Baseline Mindfulness Levels at 8 weeksChange from baseline to 8 weeksThe Five Facet Mindfulness Questionnaire-Revised, minimum 39, maximum 195, higher scores mean better outcome.
Change from Baseline Visual-Motor Coordination at 8 weeksChange from baseline to 8 weeksDigit-Symbol-Coding Test, minimum 0, maximum 133, higher scores mean better outcome.
Change from 8 weeks Mindfulness Levels at 3 monthsChange from 8 weeks to 3 monthsThe Five Facet Mindfulness Questionnaire-Revised, minimum 39, maximum 195, higher scores mean better outcome.
Change from 8 weeks Visual-Motor Coordination at 3 monthsChange from 8 weeks to 3 monthsDigit-Symbol-Coding Test, minimum 0, maximum 133, higher scores mean better outcome.

Countries

Hong Kong

Contacts

PRINCIPAL_INVESTIGATORJingxia Lin, PhD

The University of Hong Kong

Outcome results

None listed

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