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NCT Number: NCT06446089

A Chinese Version of the Thinking Health Program for East Asian Pregnant Immigrant People in Canada

The goal of this study is to determine the feasibility of using a psychosocial intervention culturally adapted in China to support perinatal mental well-being of Chinese immigrant pregnant women in Canada. The intervention is adapted from the Thinking Healthy Program (THP), available through a mobile application, and will be offered to Chinese immigrant pregnant women (22 weeks' gestation or greater) residing in Canada, who are over the age of 18, and speak Mandarin. The main questions this study aims to answer are:

* Will the Chinese version of the THP be acceptable to Chinese immigrant pregnant women residing in Canada and will they use the program which is delivered through a mobile App? * How well does the process of recruiting, keeping participants in the study and helping them complete the activities work, so it can be used for a future larger study?

Women interested in the study and who meet the study criteria will complete a questionnaire at the start of the study, then use the THP for three weeks, complete questionnaires 3-4 weeks after completing the intervention and 6-8 weeks after having their baby(ies). Some may be asked to participate in an individual interview.

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Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Queen's University

Kingston, Ontario, K7L 3N6, Canada

Location status: Recruiting

Location contact

Shahirose S Premji, NP, PhD

CONTACT

[email protected]

1-613-533-6000 ext. 79885

About this study

Common mental health conditions during pregnancy include depression and anxiety. Having an immigrant status and belonging to an ethnic minority group is linked to an increased likelihood of perinatal mental health problems. The lack of culturally tailored and innovative intervention is a predominant factor affecting mental health outcomes for immigrant women. Psychological and psychosocial interventions have been reported to significantly improve non-migrant women's mental health. The Thinking Healthy Program (THP), a low-intensity, low-cost, psychosocial intervention ("talking therapies") based on cognitive behavioural therapy, is comprised of 12, 1-hour sessions with content organized in modules (e.g., preparing for the baby, baby's arrival) that have associated activities (e.g., mood chart). In China, the THP has been culturally and linguistically adapted using rigorous processes and delivered to support women in the management of perinatal depression. To improve access and ensure a more impactful outcome to the culturally adapted THP, a mobile App was created in China with a brief Chinese version of the culturally adapted THP.

The primary objective of this study is to (1) assess the feasibility (acceptability and usability) of the linguistically and culturally adapted THP delivered through a mobile App to Chinese immigrant pregnant women residing in Canada; and (2) examine the process of recruitment, retention, and adherence to intervention to inform a future trial. The secondary objective is to produce preliminary evidence on the effectiveness of the brief Chinese version of THP on immigrant women's mental well-being, specifically depression.

A sequential explanatory mixed-method feasibility study involving a pre-post design in which a single group will be assembled and assessed quantitatively at baseline, 3-4 weeks after initiation of brief Chinese version of the THP intervention and again at 6-8 weeks following the birth of their baby. A subset of participants that have engaged with the intervention (n=up to 15) will be invited to individual semi-structured telephone interview to share their experience with the intervention.

A convenience sample of 50 participants will be recruited for the intervention, with a subset of 15 participants to be individually interviewed via the telephone.

Participants will be recruited through social media (WeChat and Xiaohongshu), research team members' University mailing list, dissemination to professional colleagues (e.g., Obstetrics and Gynecologists), and collaboration with social and health-based organizations that serve the East Asian community in Canada.

At baseline, the sociodemographic characteristics, immigrant characteristics, health/obstetric history, and history of psychological well-being will be assessed. Potential covariates that will be assessed once include acculturation (baseline; Vancouver Index of Acculturation) and preterm birth (at 6 to 8 weeks postpartum) while all others including pregnancy-related anxiety (Pregnancy-Related Anxiety Scale), depression severity (Patient Health Questionnaire-9), somatic symptoms (Patient Health Questionnaire-15), psychological stress (Perceived Stress Scale-10), resilience (Connor-Davidson Resilience Scale-10), social support (Multidimensional Scale of Perceived Social Support), mother-infant relationship (prenatal section of the Pre- and Postnatal Bonding Scale), and patient activation (Behavioural Activation for Depression Scale) will be assessed at baseline and follow-up (3-4 weeks after initiation of intervention and/or 6 to 8 weeks post-partum), using the scales and instruments listed above.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • pregnant women at ≥ 22 weeks of gestation; AND
  • ≥ 18 years old; AND
  • are first or second-generation Chinese immigrants residing in Canada (who identify as someone with East Asian cultural and ethnic background born outside of Canada or have at least one parent born outside of Canada); AND
  • understand both spoken and written Mandarin language; AND
  • have access to internet and a smartphone with Android operating system or willing to download an Android emulator to operate the App; AND
  • are willing to download and use the study mobile App with brief Chinese version of THP for "talking therapy" with accompanying activities.

Exclusion criteria

  • Women currently being treated for mental conditions, including depression

Treatment and study plan

THP: cognitive behavior therapy and behavioral activation

Behavioral

The adapted THP takes into account cultural and linguistic characteristics of the participants. Participants will be invited to complete three modules on an Android based app on their mobile, populated with information and activities from the adapted THP.

Primary outcomes

  1. Score on the System Usability Scale (SUS) 10 points

    Time frame: 3-4 weeks after initiation of intervention

    Objective measurement of usability of internet-based cognitive behavioural therapy

  2. Acceptability of app-based THP

    Time frame: 3-4 weeks after initiation of intervention

    Structured questions based on seven domains of Sekhon's Theoretical Framework of Acceptability

  3. Recruitment to study

    Time frame: During recruitment to study, expected 4 months

    Through RedCap-captured data and study intervention App-derived user data. Number of participants approached and recruited to the study will be tracked, and reported in a participant flow diagram.

  4. Retention in study

    Time frame: Through study completion, an average of 12 months.

    Number of participants lost to follow-up (i.e., these may include dropouts who use the brief Chinese version of the THP mobile App but fail to complete the follow-up assessments), as well as number of participants with partial or complete data for analysis will be tracked.

  5. Adherence to intervention

    Time frame: Through intervention duration, an average of 3-4 weeks.

    Defined as the extent to which individuals experience the content of the brief Chinese version of the THP mobile App (i.e., average amount of time participants spend on the modules, average amount of time participants use of the health assistants and tools within the app). Measured through App-derived user data.

Secondary outcomes

  1. Effectiveness of app-based THP

    Time frame: Baseline, 3-4 weeks after initiation of intervention, and 6-8 weeks post-partum

    Edinburgh Postnatal depression scale (EPDS; 10 items). Assess change of mean scores from baseline to treatment completion (at 3-4 weeks), and 6-8 weeks after the birth of the baby, adjusting for significant predictors (e.g. social support, mother-infant bonding).

Other outcomes

  1. Pregnancy-related anxiety

    Time frame: Baseline, & 3-4 weeks after initiation of intervention

    Pregnancy-Related Anxiety Scale (10 items)

  2. Somatic symptoms

    Time frame: Baseline, 3-4 weeks after initiation of intervention, and 6-8 weeks post-partum

    PHQ-15 (14 items)

  3. Psychological stress

    Time frame: Baseline, 3-4 weeks after initiation of intervention, and 6-8 weeks post-partum

    Perceived Stress Scale (10 items)

  4. Resilience

    Time frame: Baseline, 3-4 weeks after initiation of intervention, and 6-8 weeks post-partum

    Connor-Davidson Resilience Scale (10 items)

  5. Social support

    Time frame: Baseline, 3-4 weeks after initiation of intervention, and 6-8 weeks post-partum

    Multidimensional Scale of Perceived Social Support (12 items)

  6. Mother-infant relationship

    Time frame: Baseline, 3-4 weeks after initiation of intervention, and 6-8 weeks post-partum

    Pre- and Postnatal Bonding Scale (5 items)

  7. Patient activation

    Time frame: Baseline & 3-4 weeks after initiation of intervention

    PREMIUM Abbreviated activation scale (5 items)

  8. Preterm birth

    Time frame: 6-8 weeks post-partum

    Pregnancy/Delivery/Puerperium Outcome questions (5 items)

  9. Acculturation

    Time frame: Baseline

    Vancouver Index of Acculturation (18 items)

  10. Depression severity

    Time frame: Baseline, 3-4 weeks after initiation of intervention, and 6-8 weeks post-partum

    Patient Health Questionnaire-9 (PHQ-9)

Study contacts

Contact information is provided by the study sponsor or research team.

Shahirose Premji, PhD, NP

CONTACT

[email protected]

613-533-6000 ext. 79885

Sponsors and collaborators

Lead sponsor

Queen's University

Other

Registry information

Official study title

The Feasibility of a Culturally Tailored Mobile App-based Thinking Healthy Program for Mental Health Support of East Asian Pregnant Immigrants in Canada

Important dates

Study start
2024
Primary completion
2025
Study completion
2025
First posted
Jun 6, 2024
Registry last updated
Jul 28, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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