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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06438484
Other study ID # NUTNS
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 1, 2023
Est. completion date June 30, 2023

Study information

Verified date May 2024
Source Nij Smellinghe Hosptial
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

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).


Description:

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.


Recruitment information / eligibility

Status Completed
Enrollment 43
Est. completion date June 30, 2023
Est. primary completion date June 30, 2023
Accepts healthy volunteers
Gender All
Age group 18 Years and older
Eligibility 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.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
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.

Locations

Country Name City State
Netherlands Nij Smellinghe hospital Drachten Friesland

Sponsors (1)

Lead Sponsor Collaborator
Nij Smellinghe Hosptial

Country where clinical trial is conducted

Netherlands, 

Outcome

Type Measure Description Time frame Safety issue
Other patiënt characteristics, age age(years) january 2023 - june 2023
Other patiënt characteristics, sex sex (male or female) january 2023 - june 2023
Other patiënt characteristics, living situation living situation(together or alone) january 2023 - june 2023
Other patiënt characteristics, BMI body mass index(BMI) january 2023 - june 2023
Other patiënt characteristics, comorbidities comorbidities(age-adjusted Charlson Comorbidity index) january 2023 - june 2023
Other patiënt characteristics, hb haemoglobin level(mmol/L) january 2023 - june 2023
Other patiënt characteristics, tumor location tumor location(rectal or colon) january 2023 - june 2023
Other patiënt characteristics, ASA ASA score(I-IV) january 2023 - june 2023
Other patiënt characteristics, surgical procedure surgical procedure (open or laparoscopic) january 2023 - june 2023
Primary Coverage Coverage was defined as 'the participation rate in the innovation by the intended audience' and was determined as the percentage of eligible patients who were assessed and able to follow the suitable prehabilitation pathway. Reasons for drop-out and non-participation were reported. january 2023 - june 2023
Primary Duration , which can be subdivided into coverage, duration, content, and frequency. Duration was measured by the number of days between assessment and surgery and should be at least thirty days. january 2023 - june 2023
Primary Content Content was measured by the number of different components of the intervention delivered. january 2023 - june 2023
Primary Frequency Frequency was measured by the percentage of times when the training intensity as prescribed, time, and the days on which nutritional requirements were achieved january 2023 - june 2023
Secondary Preoperative aerobic capacity Preoperative aerobic capacity was measured before and after the prehabilitation program by the Steep Ramp Test. The maximum wattage will be reported. january 2023 - june 2023
Secondary Preoperative nutritional status Preoperative risk of malnutrition was measured before and after the prehabilitation program by the the patient generated subjective global assessment short form (PG-SGA SF). This is a validated instrument used by dietitians for the assessment of malnutrition and monitoring of interventions. A low score means a low risk of malnutrition. january 2023 - june 2023
Secondary Complications The occurrence of complications was reported, and complications were categorized according to the Clavien-Dindo classification. january 2023 - june 2023
Secondary Length of stay Length of stay was defined as days admitted to the hospital2. january 2023 - june 2023
Secondary Time to recovery of physical functioning Time to recovery of physical functioning was measured by the modified Iowa level of assistance scale (mILAS) and was reported as time in days between surgery and full inhospital recovery of physical functioning. january 2023 - june 2023
Secondary Facilitation strategies Facilitation strategies are strategies to optimize implementation aimed at barriers known from previous research, which are logistical and financial challenges. The physiotherapist, dietitian and embedded researcher documented their observations on influencing factors in a logbook. january 2023 - june 2023
Secondary Practitioner responsiveness Practitioner responsiveness is defined as 'engagement to the intervention'. Practitioner responsiveness was measured by a short questionnaire for the physiotherapist and dietitian based on a measurement instrument for determinants of innovation at the end of the study period. Participant responsiveness was measured by a short questionnaire after finishing their prehabilitation program, based on questionnaires in comparable studies january 2023 - june 2023
Secondary Participant responsiveness Participant responsiveness is defined as 'engagement to the intervention'. Participant responsiveness was measured by a short questionnaire after finishing their prehabilitation program, based on questionnaires in comparable studies january 2023 - june 2023
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