Trial · NCT07902141
A Web-based Intervention Program for Postpartum Depression
NCT07902141, Early phase 1, Recruiting, Babes-Bolyai University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. A Web-based Intervention Program for Postpartum Depression. Trials, record NCT07902141. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07902141
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- A Web-based Intervention Program for Postpartum Depression
- NCT number
- NCT07902141
- Status
- Recruiting
- Phases
- Early phase 1
- Enrollment
- 30 participants, estimated
- Lead sponsor
- Babes-Bolyai University
- Conditions
- Postpartum Depression (PPD), Web-based Intervention
- Interventions
- Web-based program for postpartum depression
- First posted
- 2026-10-28
- Last updated
- 2026-10-28
Source ClinicalTrials.gov
Registered outcomes10
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Program Usability | post-test (immediately following the third group meeting and the completion of the five mandatory modules) | The System Usability Scale - scores can range from 0 (indicating very low perceived usability) to 100 (indicating excellent perceived usability) |
| Primary | Program Usability | post-test (immediately following the third group meeting and the completion of the five mandatory modules), during a scheduled session dedicated to administering the semi-structured interview | A semi-structured interview - the responses will be transcribed and analyzed to derive conclusions regarding the program's perceived usability and to identify specific suggestions for further improvements |
| Primary | Participant Engagement | post-test (immediately following the third group meeting and the completion of the five mandatory modules), during a scheduled session dedicated to administering the semi-structured interview | A semi-structured interview - the responses will be transcribed and analyzed to derive conclusions regarding the program's perceived engagement and to identify specific suggestions for further improvements |
| Secondary | Postpartum Depression | baseline, post-test (immediately following the third group meeting and the completion of the five mandatory modules), and one-month follow-up (one month after program completion) | The Edinburgh Postnatal Depression Scale - scores range from 0 to 30, with higher scores indicating a higher level of symptom severity |
| Secondary | Postpartum Depression | baseline, post-test (immediately following the third group meeting and the completion of the five mandatory modules), and one-month follow-up (one month after program completion) | Patient Health Questionnaire (9-item version) - scores range from 0 to 27, with higher scores indicating a more severe level of symptoms |
| Secondary | Anxiety | baseline, post-test (immediately following the third group meeting and the completion of the five mandatory modules), and one-month follow-up (one month after program completion) | Generalized Anxiety Disorder-7 - scores range from 0 to 21, with higher scores indicating a higher level of symptom severity |
| Secondary | Rigid attitudes toward motherhood | baseline, post-test (immediately following the third group meeting and the completion of the five mandatory modules), and one-month follow-up (one month after program completion) | The Attitudes Toward Motherhood Scale - scores range from 0 to 60, with higher score indicating more dysfunctional or rigid beliefs regarding motherhood |
| Secondary | Psychological flexibility | baseline, post-test (immediately following the third group meeting and the completion of the five mandatory modules), and one-month follow-up (one month after program completion) | The 7-item Acceptance and Action Questionnaire-II - scores range from 7 to 49, with higher scores indicating greater psychological inflexibility, experiential avoidance, and more potential psychological distress. Lower total scores mean more psychological flexibility. |
| Other | Satisfaction with the program | post-test (immediately following the third group meeting and the completion of the five mandatory modules) | The Client Satisfaction Questionnaire - scores range from 8 to 32, with higher scores indicating greater satisfaction |
| Other | Completion rate | post-test (immediately following the third group meeting and the completion of the five mandatory modules) | Percentage of participants who completed at least 5 modules |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers6
The papers the trial lists on ClinicalTrials.gov.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT07902141
GET https://conductscience.org/api/trials/v1/NCT07902141/registered