The Challenges of Evidence-based Prehabilitation in a Real-life Context for Patients Preparing for Colorectal Surgery

NCT ID: NCT06438484

Last Updated: 2024-06-03

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

43 participants

Study Classification

OBSERVATIONAL

Study Start Date

2023-01-01

Study Completion Date

2023-06-30

Brief Summary

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Background: Multimodal prehabilitation programs are effective in reducing complications after colorectal surgery in patients with high risk of postoperative complications due to low aerobic capacity and/or malnutrition. However, high implementation fidelity is needed to achieve these effects in real-life practice. Therefore, this study aimed to investigate the implementation fidelity of an evidence-based prehabilitation program in the real-life context of a regional hospital.

Methods: In this observational cohort study with multiple case analysis, we enrolled all patients who underwent surgery for colorectal cancer from January 2023 to June 2023, in one Dutch peripheral hospital. Patients meeting criteria for low aerobic capacity or malnutrition were advised to participate in a personalized prehabilitation program. Implementation fidelity was investigated on four domains; 1) coverage (participation rate), 2) duration (number of days following the prehabilitation program), 3) content (delivery of prescribed intervention modalities), and 4) frequency (attendance of sessions and compliance with prescribed parameters). An aggregated percentage of content and frequency was calculated to determine overall adherence. The intended outcomes were improvement in preoperative aerobic capacity and malnutrition, and improved postoperative recovery (i.e., reducing complications, length of stay, and time to functional recovery).

Detailed Description

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Study design and patients This observational cohort study was conducted from January 2023 to June 2023 with case analysis on the high-risk patients following the prehabilitation program in Nij Smellinghe (NS). The study was approved by the Local Ethic Committee of NS. The first author was a physiotherapist, who acted as an embedded scientist in the colorectal pathway25. For the period of this study, only one physiotherapist and dietitian performed the prehabilitation program to prevent provider-dependent bias. All patients, both high-risk and low-risk, of 18 years or older scheduled for elective colorectal surgery in NS were asked for their informed consent to be included in the cohort. No exclusion criteria were applied. The STrengthening the Reporting of Observational Studies in Epidemiology (STROBE) guideline for reporting observational studies was followed26.

Study setting NS is a regional hospital with 339 beds in The Netherlands, where annually 150 patients undergo colorectal surgery27. NS is an innovative hospital in the field of perioperative care and the Enhanced Recovery After Surgery (ERAS) protocol has been implemented into usual care since 201828. In January 2023, following new scientific insights, an evidence-based multimodal prehabilitation program was implemented in the colorectal pathway. This pathway included assessment of patients on their risk of postoperative complications and offering a multimodal prehabilitation program for high-risk patients.

Preoperative risk assessment When patients were indicated for colorectal surgery, a physiotherapist and dietitian conducted risk assessment for postoperative complications. Patients meeting criteria for low aerobic capacity and/or high risk of malnutrition were advised to participate in a personalized prehabilitation program2,29.

The physiotherapist assessed aerobic capacity. Aerobic capacity was measured by the cardiopulmonary exercise test (CPET) or modified steep ramp test (SRT), following the protocol of previous research on preoperative risk assessment2,15,30. Patients with a low aerobic capacity, indicated by a work at peak exercise achieved at the modified SRT ≤1.5W/kg or an oxygen uptake at the VAT ≤11mL/kg/min at the CPET, were indicated as high-risk patients.

The dietitian evaluated risk of malnutrition by using the Patient-Generated Subjective Global Assessment Short Form (PG-SGA SF). Based on the Global Leadership Initiative on Malnutrition (GLIM) criteria, patients were diagnosed with malnutrition, thus indicating the nutrition-modality of prehabilitation31. According to the GLIM-criteria, malnutrition is defined as the presence of one phenotypic criterion (non-volitional weight loss, low body mass index, and reduced muscle mass) and one etiologic criterion (reduced food intake or assimilation, and inflammation or disease burden)32. Muscle mass and body composition was assessed with the bioelectrical impedance analysis (BIA) (Bodygram Plus, Akern, Italy).

Patients with high-risk profile: multimodal prehabilitation program High-risk patients followed an evidence-based multimodal prehabilitation program for five weeks, incorporating modalities tailored to address their impairments2,12,15. Patients performed physical exercise training and/or received dietary counseling for five weeks, provided by a trained physiotherapist and dietitian (both \>15 years experience). The physical exercise training consisted of high-intensity interval training (HIIT) three times a week and functional strengthening exercises. Patients visited the hospital two times a week and performed home exercise training five times a week on a stationary cycle ergometer (Corival Home+, Lode BV, Groningen, The Netherlands).

The dietary intervention consisted of optimization of energy and protein intake, optimization of timing of eating protein-rich products, and if necessary additional protein and vitamin supplements. Individual protein requirements were set at 1.5-1.9 g/kg fat free mass. Patients used the eiFIT-application or a food diary to track their protein intake33.

Treating patients with low hemoglobin levels, offering alcohol- and smoking cessation interventions, and giving psychological support were also elements of the prehabilitation program in NS. However, this is already part of usual care since implementation of the ERAS-protocol and therefore not specifically evaluated in this study. A detailed description of the complete pathway is provided in Appendix 1.

Statistical analysis All data were analyzed using descriptive statistics. For patient characteristics continuous data were tested for normality by the Shapiro-Wilk test and QQ-plot. Median and interquartile range (IQR) or mean and standard deviation were reported accordingly. To report the fidelity of the prehabilitation program, absolute values and percentages were given. To prevent selection bias, NS reimbursed the expenses of prehabilitation for people who otherwise could not afford it, as insurance companies did not reimburse prehabilitation in The Netherlands during the study period. Data were analyzed using R Framework 4.2.2 for macOS (version 2022, Vienna)42.

Conditions

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Colorectal Surgery

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Low risk

Patients with high aerobic capacity and good nutritional status were given the advice to eat healthy and stay active until surgery. Postoperative data were collected for evaluative purposes.

No interventions assigned to this group

High risk

High-risk patients followed an evidence-based multimodal prehabilitation program for five weeks, incorporating modalities tailored to address their impairments. Patients performed physical exercise training and/or received dietary counseling for five weeks, provided by a trained physiotherapist and dietitian (both \>15 years experience).

multimodal prehabilitation program

Intervention Type BEHAVIORAL

Patients performed physical exercise training and/or received dietary counseling for five weeks, provided by a trained physiotherapist and dietitian (both \>15 years experience). The physical exercise training consisted of high-intensity interval training (HIIT) three times a week and functional strengthening exercises. Patients visited the hospital two times a week and performed home exercise training five times a week on a stationary cycle ergometer (Corival Home+, Lode BV, Groningen, The Netherlands).

The dietary intervention consisted of optimization of energy and protein intake, optimization of timing of eating protein-rich products, and if necessary additional protein and vitamin supplements. Individual protein requirements were set at 1.5-1.9 g/kg fat free mass. Patients used the eiFIT-application or a food diary to track their protein intake.

Interventions

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multimodal prehabilitation program

Patients performed physical exercise training and/or received dietary counseling for five weeks, provided by a trained physiotherapist and dietitian (both \>15 years experience). The physical exercise training consisted of high-intensity interval training (HIIT) three times a week and functional strengthening exercises. Patients visited the hospital two times a week and performed home exercise training five times a week on a stationary cycle ergometer (Corival Home+, Lode BV, Groningen, The Netherlands).

The dietary intervention consisted of optimization of energy and protein intake, optimization of timing of eating protein-rich products, and if necessary additional protein and vitamin supplements. Individual protein requirements were set at 1.5-1.9 g/kg fat free mass. Patients used the eiFIT-application or a food diary to track their protein intake.

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* a patient must be awaiting CRC surgery in NS
* be 18 years or older

Exclusion Criteria

* Patient data will only be excluded if they do not permit the usage of their data.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Nij Smellinghe Hosptial

OTHER

Sponsor Role lead

Responsible Party

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Aletta Danielle Talen

Mac clinical health scientist

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Aletta Danielle Talen, drs

Role: PRINCIPAL_INVESTIGATOR

Nij Smellinghe

Locations

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Nij Smellinghe hospital

Drachten, Provincie Friesland, Netherlands

Site Status

Countries

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Netherlands

References

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Talen AD, van Meeteren NLU, Barten JA, Pereboom I, Krijnen WP, Jager-Wittenaar H, Bongers BC, van der Sluis G. The challenges of evidence-based prehabilitation in a real-life context for patients preparing for colorectal surgery-a cohort study and multiple case analysis. Perioper Med (Lond). 2025 Jan 17;14(1):7. doi: 10.1186/s13741-024-00481-w.

Reference Type DERIVED
PMID: 39825452 (View on PubMed)

Other Identifiers

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NUTNS

Identifier Type: -

Identifier Source: org_study_id

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