Trial · NCT07897942
Evaluation of Preoperative Anxiety in Digestive Surgery
NCT07897942, Recruiting, University Hospital, Rouen
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Evaluation of Preoperative Anxiety in Digestive Surgery. Trials, record NCT07897942. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07897942
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Evaluation of Preoperative Anxiety in Digestive Surgery
- NCT number
- NCT07897942
- Status
- Recruiting
- Enrollment
- 300 participants, estimated
- Lead sponsor
- University Hospital, Rouen
- Conditions
- Digestive System Neoplasms, Anxiety
- First posted
- 2026-10-27
- Last updated
- 2026-10-27
Source ClinicalTrials.gov
Registered outcomes19
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Major postoperative complications at day 90 assessed using the Comprehensive Complication Index (CCI) (CCI) | day 90 after surgery | Major postoperative complications will be defined as a Comprehensive Complication Index (CCI) score ≥30 at Day 90 after surgery. The association between preoperative anxiety and major postoperative complications will be assessed. The CCI ranges from 0 to 100, with higher scores indicating greater postoperative morbidity. |
| Secondary | Postoperative complications according to the Clavien-Dindo classification | 30 days and 90 days after surgery | The occurrence and severity of postoperative complications will be assessed using the Clavien-Dindo classification, which grades complications from Grade I to Grade V, with higher grades indicating greater severity. |
| Secondary | Prevalence of anxiety assessed using the State-Trait Anxiety Inventory, Form Y (STAI-Y), State scale | Preoperatively, and on Days 3, 7, 30 and 90 after surgery | The prevalence of anxiety will be assessed using the State scale of the State-Trait Anxiety Inventory, Form Y (STAI-Y). The State scale consists of 20 items and yields a score ranging from 20 to 80. A score ≥46 will indicate anxiety symptoms. |
| Secondary | Prevalence of anxiety assessed using the State-Trait Anxiety Inventory, Form Y (STAI-Y), Trait scale | Preoperatively, and on Days 3, 7, 30 and 90 after surgery | The prevalence of anxiety will be assessed using the Trait scale of the State-Trait Anxiety Inventory, Form Y (STAI-Y). The Trait scale consists of 20 items and yields a score ranging from 20 to 80. A score ≥46 will indicate anxiety symptoms. |
| Secondary | Prevalence of anxiety symptoms assessed using the Hospital Anxiety and Depression Scale (HADS), Anxiety subscale | Preoperatively, and on Days 3, 7, 30 and 90 after surgery | Anxiety symptoms will be assessed using the Anxiety subscale of the Hospital Anxiety and Depression Scale (HADS). The subscale consists of 7 items scored from 0 to 3, yielding a total score ranging from 0 to 21. A score ≥8 will indicate anxiety symptoms. |
| Secondary | Prevalence of depressive symptoms assessed using the Hospital Anxiety and Depression Scale (HADS), Depression subscale | Preoperatively, and on Days 3, 7, 30 and 90 after surgery | Depressive symptoms will be assessed using the Depression subscale of the Hospital Anxiety and Depression Scale (HADS). The subscale consists of 7 items scored from 0 to 3, yielding a total score ranging from 0 to 21. A score ≥8 will indicate depressive symptoms. |
| Secondary | Patient activation assessed using the 13-item Patient Activation Measure (PAM-13) | Preoperatively, and on Days 7, 30 and 90 after surgery | Patient activation will be assessed using the 13-item Patient Activation Measure (PAM-13), which evaluates patients' knowledge, skills and confidence in managing their health. The evolution of patient activation over time and its association with anxiety and depressive symptoms will be evaluated. |
| Secondary | Health-related quality of life assessed using the 36-Item Short Form Health Survey (SF-36) | Preoperatively, and on Days 30 and 90 after surgery | Health-related quality of life will be assessed using the 36-Item Short Form Health Survey (SF-36). |
| Secondary | Use of anxiolytic medications | Preoperatively, on postoperative Days 3 and 7 | Use of anxiolytic medications will be recorded from the medical record. |
| Secondary | Use of hypnotic medications | Preoperatively, on postoperative Days 3 and 7 | Use of hypnotic medications will be recorded from the medical record. |
1 to 10 of 19Source ClinicalTrials.gov
See all 19 registered outcomesOutcomes0
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/NCT07897942
GET https://conductscience.org/api/trials/v1/NCT07897942/registered