Trial · NCT07896174
Resistance vs Aerobic Prehabilitation Before Colorectal Cancer Surgery
NCT07896174, Not applicable, Recruiting, Semmelweis University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Resistance vs Aerobic Prehabilitation Before Colorectal Cancer Surgery. Trials, record NCT07896174. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07896174
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Resistance vs Aerobic Prehabilitation Before Colorectal Cancer Surgery
- NCT number
- NCT07896174
- Status
- Recruiting
- Phases
- Not applicable
- Enrollment
- 480 participants, estimated
- Lead sponsor
- Semmelweis University
- Conditions
- Colorectal Cancer, Colorectal Neoplasms, Postoperative Complications
- Interventions
- Resistance Training Prehabilitation, Aerobic Training Prehabilitation, Standard Trimodal Care
- First posted
- 2026-10-26
- Last updated
- 2026-10-26
Source ClinicalTrials.gov
Registered outcomes11
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Postoperative Morbidity Within 30 Days | From surgery to postoperative day 30 | Proportion of participants with any postoperative complication within 30 days after surgery. Complications are graded according to the Clavien-Dindo classification (grade I-V), and the severity distribution will also be reported. |
| Primary | Early Postoperative Morbidity Within 7 Days | From surgery to postoperative day 7 | Proportion of participants with any postoperative complication within 7 days after surgery, graded according to the Clavien-Dindo classification (grade I-V). |
| Secondary | Postoperative Mortality | Postoperative day 7 and day 30 | All-cause mortality within 7 and 30 days after surgery. |
| Secondary | Change in 6-Minute Walk Distance | At enrollment, the day before surgery (after 4-6 weeks of prehabilitation), and 8 weeks after surgery | Distance walked in 6 minutes (meters), measured by the 6-minute walk test. |
| Secondary | Change in Handgrip Strength | At enrollment, the day before surgery (after 4-6 weeks of prehabilitation), and 8 weeks after surgery | Maximal handgrip strength (kg) measured with a hand dynamometer. |
| Secondary | Change in 1-Minute Sit-to-Stand Test | At enrollment, the day before surgery (after 4-6 weeks of prehabilitation), and 8 weeks after surgery | Number of sit-to-stand repetitions completed in 1 minute. |
| Secondary | Change in Health-Related Quality of Life (SF-36) | At enrollment, the day before surgery (after 4-6 weeks of prehabilitation), and 8 weeks after surgery | 36-Item Short Form Survey; scores range from 0 to 100, higher scores indicate better health status. |
| Secondary | Change in Gastrointestinal Quality of Life (GIQLI) | At enrollment, the day before surgery (after 4-6 weeks of prehabilitation), and 8 weeks after surgery | Gastrointestinal Quality of Life Index; total score ranges from 0 to 144, higher scores indicate better quality of life. |
| Secondary | Length of Hospital Stay | From surgery to discharge, up to 30 days | Number of days from surgery to hospital discharge. |
| Secondary | Length of Intensive Care Unit Stay | From surgery to discharge, up to 30 days | Number of days spent in the intensive care unit after surgery, excluding high dependency unit stay. |
1 to 10 of 11Source ClinicalTrials.gov
See all 11 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.
Papers2
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/NCT07896174
GET https://conductscience.org/api/trials/v1/NCT07896174/registered