Trial · NCT07909512
The Effect of Home Visits in Postnatal Care on Perceived Social Support and Quality of Recovery
NCT07909512, Not applicable, Completed, Istanbul University - Cerrahpasa
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. The Effect of Home Visits in Postnatal Care on Perceived Social Support and Quality of Recovery. Trials, record NCT07909512. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07909512
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- The Effect of Home Visits in Postnatal Care on Perceived Social Support and Quality of Recovery
- NCT number
- NCT07909512
- Status
- Completed
- Phases
- Not applicable
- Enrollment
- 120 participants, actual
- Lead sponsor
- Istanbul University - Cerrahpasa
- Conditions
- Home Visit, Social Support, Postnatal Recovery
- Interventions
- Postpartum Home Visit-Based Midwife Support Program, Standard Postpartum Care
- First posted
- 2026-11-02
- Last updated
- 2026-11-02
Source ClinicalTrials.gov
Registered outcomes2
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Perceived Social Support | Before the intervention and on the 42nd day (6th week) postpartum | The Multidimensional Scale of Perceived Social Support was used to determine the level of social support perceived by mothers. Developed by Zimet et al., this scale assesses the support an individual perceives from their social environment. The scale consists of 12 items, which are rated on a seven-point Likert-type scale ranging from 1 ("strongly disagree") to 7 ("strongly agree"). It comprises three subscales-support from family, support from friends, and support from a significant other-with four items in each subscale. The total score on the scale ranges from 12 to 84, with higher scores indicating a higher level of perceived social support. |
| Secondary | Postpartum Recovery | Before the intervention and on the 42nd day (6th week) postpartum | The Quality of Postpartum Recovery Scale (QPRS) was used to assess the quality of postpartum recovery among mothers. This scale was adapted into Turkish by Önal et al. (2023). Consisting of 11 items in total, the scale comprises two subdimensions: "evaluations regarding the last 24 hours" (items 1-5) and "current status" (items 6-11). The items are rated using an 11-point Likert-type scale, with scores ranging from 0 to 10. The first subdimension is reverse-scored, while the second subdimension is scored directly. The total score for the first subdimension ranges from 0 to 50, and the total score for the second subdimension ranges from 0 to 60. In the interpretation of the scale scores, higher scores indicate a better quality of postpartum recovery. |
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.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
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/NCT07909512
GET https://conductscience.org/api/trials/v1/NCT07909512/registered