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Digital Home-Based Prehabilitation Before Surgery

Digital Home-Based Prehabilitation Before Surgery

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06231576
Acronym
dHOPE
Enrollment
140
Registered
2024-01-30
Start date
2024-02-01
Completion date
2030-12-31
Last updated
2024-01-30

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

Conditions

Cancer Colorectal, Frailty, Surgery

Keywords

Prehabilitation, Colorectal cancer, Frailty

Brief summary

This clinical trial compares two different prehabilitation programs, with no organized prehabilitation, prior to major colorectal cancer surgery. The prehabilitation programs include intensive and coached physical exercise and optimized nutritional intake coupled with smoking cessation, physiological support and correction of poly-pharmacy.

Detailed description

Patients are randomized to either a digital home-based program, a physical hospital-based program or no-organized prehabilitation. The eligible patients are anyone scheduled for colorectal cancer surgery who are fluent in Norwegian able to consent and to understand questionnaires. The main question the study aims to answer is whether a digital home-based program is non-inferior to a hospital-based program in terms of improved physical capacity and maintenance of life-quality. In addition, blood samples will be drawn at three time points, at inclusion, after intervention (prior to surgery) and 6 weeks after surgery to analyze and search for biomarkers reflecting patients' individual surgical risk profile and response to prehabilitation. Participants randomized to intervention, will be given psychological coaching and support, individualized nutritionist counselling, coached, structured and repeated 60 minutes daily exercises for three weeks prior to surgery. The control group will receive no organized prehabilitation in the period of time between diagnose and surgery.

Interventions

OTHERPrehabilitation

* Nutritional optimization: A nutritionist will perform a structured interview, comprehensive nutrition assessment, and provide personalized dietary advice. The main goal is to ensure optimal protein intake to support exercise-induced anabolism. A daily protein intake of 1.2-2.0 g/kg will meet needs as outlined in surgical nutrition guidelines. * Exercise: Based on current guidelines and instructed by a dedicated physiotherapist, for 1 hour per day preoperatively to increase muscle strength, aerobic capacity and physical endurance. Intensity will be based on the rate of perceived exertion using the Borg scale, a 15-graded scale ranging from very light to very hard. Resistance exercises will target upper/lower body, and abdominal muscles. * Psychological coaching and support: Performed as one interview during inclusion, followed by weekly phone calls by a study nurse coordinator during the preoperative intervention.

Sponsors

Diakonhjemmet Hospital
CollaboratorOTHER
Vestre Viken Hospital Trust
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Planned for major gastrointestinal cancer surgery * Fluent in Norwegian and able to consent and to understand questionnaires

Exclusion criteria

* Inability to walk for six minutes or to rise independently from a chair * Inability to comprehend exercise program or to comply with written and oral instructions * Presence of a cardio-pulmonary condition that precludes exercise * Living in very remote areas making a hospital-based intervention group impossible to implement * Being without a permanent address * Admittance to a hospital facility for \> 50% of the time from diagnosis to surgery

Design outcomes

Primary

MeasureTime frameDescription
6MWTAt inclusion, prior to intervention. After intervention, prior to surgery. 4-6 weeks after surgeryDistance (in meters) walked in 6 minutes

Secondary

MeasureTime frameDescription
European Organisation for Research and Treatment of Cancer Core Quality of Life questionnaireAt inclusion, prior to intervention. After intervention, prior to surgery. 4-6 weeks after surgeryThe EORTC Core Quality of Life questionnaire (EORTC QLQ-C30) is designed to measure cancer patients' physical, psychological and social functions. The questionnaire range from 0 to 100; a higher score represents a higher (better) level of functioning, or a higher (worse) level of symptoms.
Generic Short Patient Experiences Questionnaire (GS-PEQ)At inclusion, prior to intervention. After intervention, prior to surgery. 4-6 weeks after surgeryGS-PEQ is a questionnaire for collecting data about user experiences across different types of services. The questionnaire has 12 questions ranging from 1-5; a higher score represents a higher (better) experience.
Mortality3 months after surgery90-day mortality
Complications3 months after surgeryComprehensive Complication Index (CCI) reflects the gravity of the overall complication burden on the patient on a scale from 0 (no complication) to 100 (death)
Need of additional health care support4-6 weeks after surgeryUse of health care support from the municipality, nursing homes etc
EuroQol Group Questionnaire 5D (EQ-5D)At inclusion, prior to intervention. After intervention, prior to surgery. 4-6 weeks after surgeryEQ-5D is a standardized measure of health-related quality of life with 5 dimensions, each dimension represented by a value 1-5 where higher value represents worse outcome.
Cost-effectiveness3 months after surgeryAn estimation of the resources used on the prehabilitation program will be compared to resources saved by shorter aLoS, less use of nursing home facilities and less need of community healthcare services
Aggregated length-of-stay (aLoS)4-6 weeks after surgeryTotal time in hospital (from surgery and any readmittance) within 30-days from surgery

Other

MeasureTime frameDescription
RNA methylationAt inclusion, prior to intervention. After intervention, prior to surgery. 4-6 weeks after surgeryBlood samples for RNA methylation profiling will be implemented in a machine learning algorithm to search for biomarkers reliably reflecting frailty and effect of prehabilitation.
MetabolomeAt inclusion, prior to intervention. After intervention, prior to surgery. 4-6 weeks after surgeryBlood samples for metabolome profiling will be implemented in a machine learning algorithm to search for biomarkers reliably reflecting frailty and effect of prehabilitation.
DNA methylationAt inclusion, prior to intervention. After intervention, prior to surgery. 4-6 weeks after surgeryBlood samples for DNA methylation profiling will be implemented in a machine learning algorithm to search for biomarkers reliably reflecting frailty and effect of prehabilitation.

Contacts

Primary ContactGuro Kleve, MD
guro.kleve@vestreviken.no+47 32 80 30 00
Backup ContactRune Ougland, MD PhD
rune.ougland@vestreviken.no+47 32 80 30 00

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026