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Physical Activity in Relation to Surgical Procedures

Physsurg - a Controlled Randomized Trial on the Effect of Physical Activity in Relation to Outcome After Surgery

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02299596
Enrollment
761
Registered
2014-11-24
Start date
2015-01-01
Completion date
2025-12-31
Last updated
2026-04-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Colorectal Cancer, Surgery

Keywords

Colorectal neoplasm, Physical activity

Brief summary

This study will compare the outcome after surgery between a group of patients that receives instructions for prehabilitation training and one group that received standard treatment.

Detailed description

The aim of this study is to investigate whether a training program with intensified physical activity prior to and after a surgical procedure reduces the surgical-related postoperative recovery time, hospital stay, sick leave and complication rate. A secondary aim is to investigate the effect of a training program with pre- and post- operative PA on the rate of resumption of QoL and normal physical function.

Interventions

OTHERPhysical activity

The intervention will take place both pre- and postoperatively. During the hospital stay both groups will be treated in the same manner.

Sponsors

Sahlgrenska University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Diagnosed colorectal cancer and a planned surgical procedure

Exclusion criteria

* HIPEC surgery, not able to give informed consent or understand the intervention

Design outcomes

Primary

MeasureTime frame
Recovery measured as physical recovery measured in questionnaire4-6 weeks

Secondary

MeasureTime frameDescription
Psychological recovery measured in a questionnaire, patient reported4-6 weeks and 1 year post-operativelyRecovery
Recovery measured as time back to work1 yearRecovery
Complications according to Clavien-Dindowithin 90 daysPostoperative complications
QoL measured using SF-364-6 weeks and 1 yearQoL according to SF-36
QoL measured using EQ-5D4-6 weeks and 1 yearQoL according to EQ-5D
QoL measured using a specifically developed instrument for this study4-6 weeks and 1 yearHealth related QoL
Mortality3 and 5 yearsLong term mortality
Re-admissions1 yearHospital re-admissions
Reoperations1 yearReoperations
Total time of hospital stay1 yearLength of stay
IGF-1 and IGFBP-34 weeks postopeartivelyLab values
Postoperative pain measured with Brief Pain Inventory-Short form4 weeksPain measured by BPI-S
Health economic analysis4 weeksHealth economic analysis modified according to results of primary outcome

Countries

Sweden

Contacts

PRINCIPAL_INVESTIGATOREva Haglind, M.D., Ph.D.

SSORG

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 28, 2026