Trial · NCT07913815
Return to Physical Activity After Retropublic Transvaginal Sling and Laparoscopic Sacrocolpopexy
NCT07913815, Active not recruiting, Public Healthcare Centre of the Ministry of Interior and Administration
3 sourcestrials-2026-11-12-0.4.0
Cite this record
ConductScience Library. Return to Physical Activity After Retropublic Transvaginal Sling and Laparoscopic Sacrocolpopexy. Trials, record NCT07913815. Release trials-2026-11-12-0.4.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07913815
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Return to Physical Activity After Retropublic Transvaginal Sling and Laparoscopic Sacrocolpopexy
- NCT number
- NCT07913815
- Status
- Active not recruiting
- Enrollment
- 200 participants, estimated
- Lead sponsor
- Public Healthcare Centre of the Ministry of Interior and Administration
- Conditions
- Stress Urinary Incontinence, Pelvic Organ Prolapse
- Interventions
- Questionnaire and Physical Exam
- First posted
- 2026-11-03
- Last updated
- 2026-11-03
Source ClinicalTrials.gov
Registered outcomes7
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Time to return to the pre-operative level of physical activity | From surgery to 6 months | Days from surgery to the end of the first diary week in which the participant reports full return ("yes") to her usual pre-operative activity level. |
| Secondary | Time to first performance of each predefined activity | From surgery to 6 months. | Days from surgery to the first performance of each of ten everyday activities, recorded on the diary date card. |
| Secondary | Early postoperative pain as a predictor of return to activity | From surgery to 6 months. | Association between mean pain intensity (NRS 0-10) on postoperative days 0-7 and time to return to the pre-operative activity level (hazard ratio). |
| Secondary | Reasons for not performing activities. | Weeks 1-6 | Proportion of coded reasons per activity and week, distinguishing adherence to medical advice from fear of harming the surgical result. |
| Secondary | Clinical factors associated with slower return to activity. | From surgery to 6 months. | Association of baseline and perioperative characteristics (e.g. age, BMI, parity, baseline activity level, operative data, complications) with time to return to the pre-operative activity level . |
| Secondary | Quality of early recovery (QoR-15) | Postoperative day 1. | QoR-15 total score, 0-150 (higher = better recovery). |
| Secondary | Satisfaction with treatment (ICIQ-S) | 6th week, 6th month. | ICIQ-S score; exploratory (working Polish translation). |
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.
Papers5
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.
Source
- Release
- trials-2026-11-12-0.4.0
- Release manifest SHA-256
- 0f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4
- Registry capture
- 2026-11-12
- Results copy, AACT
- 2026-03-23
- NIH clinical studies file
- 2026-11-13
Source ClinicalTrials.gov
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNone 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/NCT07913815
GET https://conductscience.org/api/trials/v1/NCT07913815/registered