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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06390735
Other study ID # N202312058
Secondary ID EHHRRB 194/2023
Status Recruiting
Phase N/A
First received
Last updated
Start date March 25, 2024
Est. completion date July 2024

Study information

Verified date April 2024
Source Taipei Medical University
Contact Lindelwa Portia Dlamini, MSc
Phone +268 78369828
Email ndedlamini@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Recruiting
Enrollment 214
Est. completion date July 2024
Est. primary completion date June 2024
Accepts healthy volunteers No
Gender Female
Age group 18 Years and older
Eligibility 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

Study Design


Intervention

Behavioral:
Mommy ReachOut Intervention
The momy reachOut intervention is a web-based psycho-education with 4 sessions, released over a two week period.

Locations

Country Name City State
Swaziland King Sobhuza II Public Health Unit Manzini
Swaziland Mbabane Government Public Health Unit Mbabane Hhohho

Sponsors (1)

Lead Sponsor Collaborator
Taipei Medical University

Country where clinical trial is conducted

Swaziland, 

Outcome

Type Measure Description Time frame Safety issue
Primary Help-seeking Intention 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. Baseline; Immediately post intervention; follow-up at 1 month post intervention
Primary Help-seeking Behavior 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. Baseline; Immediately post intervention; follow-up at 1 month post intervention
Secondary Antenatal depressive symptoms Edinburgh Postnatal Depression Scale - A set of 10 items are used to measure antenatal depressive symptoms on a 4-point Likert scale (0-3). The overall score ranges from 0 to 30 and is computed by summing up all item scores. A high sum of scores indicates a high level of depressive symptoms. Baseline; Immediately post intervention; follow-up at 1 month post intervention
Secondary Health belief Theory of Planned Behavior questionnaire - The tool has 13 items that rate the constructs of the theory of planned behavior on a 5-point Likert scales (strongly disagree to strongly agree). The possible score ranges from 13 to 65, with higher scores indicating more favorable attitudes towards help-seeking, greater subjective norms to seek help, and more control over one's behavior. Baseline; Immediately post intervention; follow-up at 1 month post intervention
Secondary Antenatal depression Stigma Depression stigma scale - The 9 items in this scale measure personal stigma towards depression. Responses to each item are measured on a five-point Likert scale (strongly disagree to strongly agree). The total score is through summing up all item scores and a total possible score ranges from 0 to 36. A higher score indicates higher levels of personal depression stigma Baseline; Immediately post intervention; follow-up at 1 month post intervention
Secondary Depression literacy Depression literacy scale - The scale measures participants knowledge of the signs of depression, risk factors, and treatment among others. participants respond to each item with a true (1) or false (0), therefore, the total possible score ranges from 0 to 22. From summing up all item scores, a higher score will indicate high antenatal depression literacy. Baseline; Immediately post intervention; follow-up at 1 month post intervention
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