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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04762914
Other study ID # 2021.038N
Secondary ID
Status Completed
Phase
First received
Last updated
Start date September 1, 2018
Est. completion date December 31, 2019

Study information

Verified date February 2021
Source Medway Primary Care Trust
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Quality Improvement Project to evaluate how prehabilitation can be incorporated into our colorectal cancer pathway and assess its clinical benefits.


Description:

The aim was to evaluate how prehabilitation (PH) can be incorporated into our colorectal cancer pathway and assess its clinical benefits. Patients underwent PH (exercise, nutrition and psychological support) before resection of colorectal carcinoma in a DGH over fourteen months. Patients were matched by operation, age, sex and ASA to non-prehabilitation (NPH) patients using a prospectively maintained database. Length of stay (LoS) and complication rate and 90-day readmission rates were compared using Wilcoxon and McNemar's methods. Prehabilitation significantly improved peak VO2 and AT. This corresponds to a reduction in predicted 30-day mortality. Despite a higher Charlson index LoS was unchanged suggesting prehabilitation may permit safe resection in comorbid patients.


Recruitment information / eligibility

Status Completed
Enrollment 52
Est. completion date December 31, 2019
Est. primary completion date December 31, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Adults over the age of 18 who had prehabilitation for colorectal cancer Exclusion Criteria: - Children - Patients who had prehabilitation but not for colorectal cancer

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Prehabilitation
Prehabilitation is a multimodal and multidisciplinary person-centred perioperative approach involving supervised exercise training, nutritional education, management of polypharmacy and psychological advice.

Locations

Country Name City State
United Kingdom Medway Hospitals NHS Trust Gillingham Kent

Sponsors (1)

Lead Sponsor Collaborator
Medway Primary Care Trust

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Length of stay Time spent in hospital From date of operation to date of discharge in number of days over a 90 day follow up period
Primary Complication rate All Clavien-Dindo complications Follow up over a period of 90 days following operation
Secondary Anaerobic threshold Measured by looking at CPET results pre- and post- prehab CPET performed before prehabilitation and after prehabilitation (median of 36 days)
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