CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 90 enrolled / 90 target
Drug / intervention
Prehabilitation program (4 week before the surgery) +2 morebehavioral
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT05379205
NCT05379205N/ACompletedHigh Momentum (2.0/mo)Completion was 11mo ago

Multidisciplinary Prehabilitation and Postoperative Rehabilitation for Avoiding Complications in Patients Undergoing Resection of Colon Cancer: ONCOFIT Study

Universidad de Granada·interventional·Posted May 18, 2022·Updated Jun 16, 2026

In Brief

A clinical study evaluating Prehabilitation program (4 week before the surgery), Postoperative program (12 week after the surgery), and 1 other intervention for Colon Cancer and Postoperative Complications. Completed, enrolled 90 participants across 1 site.

Signals

Enrolling ahead of pace

Detailed Summary

ONCOFIT is a randomized clinical trial with a two-arm parallel design aimed at determining the influence of a multidisciplinary prehabilitation + postoperative program on post-surgery complications in patients undergoing resection of colon cancer. This intervention will include supervised physical exercise, dietary behavior change, and psychological support comparing its influence to the standard care.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesSpain

Timeline

N/ACompletedFinished
2023202420252026
First PostedMay 18, 2022
Enrollment StartNov 1, 2022
Primary CompletionJul 17, 2025
Study CompletionApr 16, 2026
TodayJul 2, 2026
Enrollment to primary: 2.7 yearsPosted 4.1 years ago

Arms & Interventions

Usual Care/Control Groupactive_comparator

Usual care group will follow the usual institutional pre-surgery care..

Other: Usual Care
Prehabilitation + Postoperative Programs (PPP) Groupexperimental

PPP group will include 3 complementary modules: (i) supervised physical exercise, (ii) dietary behavior change, and (iii) psychological support.

Behavioral: Prehabilitation program (4 week before the surgery)Behavioral: Postoperative program (12 week after the surgery)

Interventions

Prehabilitation program (4 week before the surgery)behavioral

This intervention will include 3 complementary modules: (i) supervised physical exercise: aerobic and strength High Intensity Interval Training (HIIT), 3 times per week (ii) dietary behavior change: nutritional talk + an informative brochure + a video summary, a session per week and (iii) psychological support: psychoeducation, written and verbal emotional expression, promotion of coping strategies, progressive muscle relaxation training, problem-solving and social skills, and self-efficacy enhancing, among others. This psychological component will also include counseling regarding smoking and alcohol cessation and sleep hygiene.

Postoperative program (12 week after the surgery)behavioral

This intervention will include 3 complementary modules: (i) supervised physical exercise: aerobic and strength High Intensity Interval Training (HIIT), 3 times per week (ii) dietary behavior change: nutritional talk + an informative brochure + a video summary, a session per week and (iii) psychological support: psychoeducation, written and verbal emotional expression, promotion of coping strategies, progressive muscle relaxation training, problem-solving and social skills, and self-efficacy enhancing, among others. This psychological component will also include counseling regarding smoking and alcohol cessation and sleep hygiene. NOTE: Both preoperative and postoperative programs will be administer to the participants assigned to the intervention group.

Usual Careother

Usual care group will follow the usual institutional pre-surgery care: (i) medication management, (ii) assessment of the surgery-derived risks, (iii) smoking cessation and peri-operative blood management. A trained nutritionist will evaluate the nutritional status of all patients at the baseline providing oral protein/vitamin supplementation, when necessary. Patients allocated to the control group will receive basic expert' advice on lifestyle changes.