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Clinical Trials/NCT03257332
NCT03257332
Withdrawn
Not Applicable

The EDFI-Cohort: Determining Early Development of Faecal Incontinence and Anorectal Muscle Function After Curative Surgery for Rectal Cancer.

Slagelse Hospital2 sites in 1 countryNovember 12, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Rectum Cancer
Sponsor
Slagelse Hospital
Locations
2
Primary Endpoint
Global health status/quality of life: EORTC QLQ-C30
Status
Withdrawn
Last Updated
5 years ago

Overview

Brief Summary

Background:

Patients treated for rectal cancer are in high risk of developing poor quality of life and faecal incontinence. Faecal incontinence has a negative impact on quality of life. However, there is limited knowledge on how to prevent it. Known exposures are ; age at surgery, gender, tumor height, pre-operative radiotherapy, surgical technique and temporary stoma. In order to evaluate the underlying mechanisms of faecal incontinence, it is central to evaluate the anorectal muscle function for sensory and motor impairment. Exposures representing different constructs in the biopsychosocial model are likewise likely to be associated with quality of life and faecal incontinence. These exposures include sexual dysfunction, urinary incontinence, fatique, physical inactivity and finding meaning in life. There are to our knowledge, no records on these relationships from prior to surgery to 2 years after. These biopsychosocial exposures are central to include when developing strategies that can prevent poor quality of life and faecal incontinence for patients treated for rectal cancer.

Purpose:

The primary purpose of the EDFI-Cohort study is to determine how several variables (surgical technique, anorectal muscle function, faecal incontinence, urinary incontinence, sexual dysfunction, fatigue, physical activity and finding meaning in life) develop over time and predicts quality of life. Secondary how it predicts LARS-score in patients with rectal cancer from prior to surgery to 2 years after primary treatment.

Methods:

We will include subjects diagnosed with rectal cancer and have received curative surgery (low anterior resection) with/without adjuvant (radiation/chemo) therapy. The cohort aim to recruit all eligible patients in a one year period. We estimate to recruit 70 patients.

Self-reported outcomes will be collected with a series of validated questionnaires that subjects will be asked to complete 6 times during the two year study at 3, 6, 12, 26 78 and 104 weeks. Outcomes include: Quality of life using (EORTC QLQ-C30) (primary outcome), (CR29) and (FA12), bowel related quality of life (LARS-score) (secondary outcome), faecal incontinence (Vaizey score), urinary incontinence (ICIQ-UI), (MLUTS/FLUTS) and (MLUTSsex/FLUTSsex), physical activity level from Danish National Health Profile and finding meaning in life (SOME).

Objective measures will be collected at 6 weeks, 6 months, 12 months and 24 months and include: Anorectal manometry that measures anorectal muscle function and rectal perception, a digital examination of anorectal muscle function using the Digital Rectal Examination Scoring System (DRESS) and the six-minute walk test a measure of submaximal exercise capacity.

We plan to analyze the EDFI-Cohort study as repeated measures with both simple and multiple linear regression models for the continuous data. We plan to adjust for known confounders and variables related to treatment.

Registry
clinicaltrials.gov
Start Date
November 12, 2019
End Date
December 31, 2022
Last Updated
5 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Slagelse Hospital
Responsible Party
Principal Investigator
Principal Investigator

Brian Clausen

Physiotherapist and PhD

Slagelse Hospital

Eligibility Criteria

Inclusion Criteria

  • Diagnosis of rectal cancer
  • Low anterior resection (e.g. not limited to total mesorectal excision (TME) or partial mesorectal excision (PME))
  • Ability to communicate in Danish
  • Adults (\> 18 years of age)
  • American Society of Anaesthesiologists (ASA) score: I-IV.

Exclusion Criteria

  • ASA score of: V-VI.

Outcomes

Primary Outcomes

Global health status/quality of life: EORTC QLQ-C30

Time Frame: 104 weeks

European Organisation for Research and Treatment of Cancer's generic core set on quality of life (EORTC QLQ-C30)

Secondary Outcomes

  • Low anterior resection syndrome(104 weeks)

Study Sites (2)

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