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Clinical Trials/NCT06390735
NCT06390735
Recruiting
N/A

Effectiveness of a Web-based Psychoeducation on Antenatal Depression Help-seeking in Eswatini

Taipei Medical University2 sites in 1 country214 target enrollmentMarch 25, 2024

Overview

Phase
N/A
Intervention
Not specified
Conditions
Help-Seeking Behavior
Sponsor
Taipei Medical University
Enrollment
214
Locations
2
Primary Endpoint
Help-seeking Behavior
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

The goal of this trial to test if a web-based psychoeducation will work in improving depression help-seeking intention and behavior among antenatal women with probable depression in Eswatini. The main question it aims to answer is:

• Does the web-based psychoeducation improve depression help-seeking intention and help-seeking behavior in antenatal women with probable depressive symptoms?

Researchers will compare this web-based psychoeducation to a waitlist control, to see if the program works in improving depression help-seeking intention and behavior during pregnancy.

  • The psychoeducation program will have a total of 4 sessions, which will be given to participants over a two-week period. two sessions will be delivered each week.
  • Participants will be asked questions before the intervention starts, immediately the intervention ends as well as after a month of completing the intervention.
Registry
clinicaltrials.gov
Start Date
March 25, 2024
End Date
July 2024
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Lindelwa Portia Dlamini

Principal Investigator

Taipei Medical University

Eligibility Criteria

Inclusion Criteria

  • Less than 30 weeks of gestation,
  • Aged 18 or above
  • With probable depression (Edinburg Postnatal depression scale; EPDS \> 10)
  • Has access to a smart phone
  • Fluent in spoken and written Siswati or English (with at least secondary school education)
  • Planning to remain in the country for the next 2 months
  • Willing to share her dominant phone number with the study team
  • Willing to participate in the intervention study

Exclusion Criteria

  • Antidepressants or other depression treatments
  • Currently enrolled in another trial

Outcomes

Primary Outcomes

Help-seeking Behavior

Time Frame: Baseline; Immediately post intervention; follow-up at 1 month post intervention

Actual Help Seeking Questionnaire - This 9 item scale uses binary responses (Yes or No) to measure actual help-seeking behavior. The total score is computed by summing up all item scores, where a higher score indicates higher help-seeking behavior. The total possible score ranges from 0 to 9.

Help-seeking Intention

Time Frame: Baseline; Immediately post intervention; follow-up at 1 month post intervention

General Help Seeking Questionnaire - This 9 item scale adopted a 3 point Likert scale (Unlikely, maybe, Likely) to measure help-seeking intention. The total score is computed by summing up all item scores, where a higher score indicates higher help-seeking intention. The total possible score ranges from 9 to 27.

Secondary Outcomes

  • Antenatal depressive symptoms(Baseline; Immediately post intervention; follow-up at 1 month post intervention)
  • Health belief(Baseline; Immediately post intervention; follow-up at 1 month post intervention)
  • Depression literacy(Baseline; Immediately post intervention; follow-up at 1 month post intervention)
  • Antenatal depression Stigma(Baseline; Immediately post intervention; follow-up at 1 month post intervention)

Study Sites (2)

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