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Acs-Tens Treatment for Faecal Incontinence: a RCT With Sham-controls

Primary Purpose

Faecal Incontinence, Faecal Incontinence With Faecal Urgency, Neuromodulation

Status
Completed
Phase
Not Applicable
Locations
Hong Kong
Study Type
Interventional
Intervention
AcuTENS
Sponsored by
Chinese University of Hong Kong
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Faecal Incontinence focused on measuring Faecal incontinence, Faecal urgency, Neuromodulation, Transcutaneous Electric Nerve Stimulation, Acupuncture

Eligibility Criteria

18 Years - 99 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients aged 18 years or above
  • Acupuncture naïve patients
  • Faecal incontinence with solid or liquid stool causing disruption of lifestyle
  • Psychological stability and suitability as determined by the investigator
  • Failed conservative or surgical treatment
  • Intact peripheral neurosensory nervous system as determined by clinical investigation
  • Able to read and write

Exclusion Criteria:

  • Major internal and/or external sphincter defect (>120 degrees of sphincter circumference)
  • Faecal impaction
  • Presence of full thickness rectal prolapse
  • Patients who have contact allergies to adhesive pads
  • Implanted pacemaker, defibrillator, cardiopathy
  • Pregnancy or intention to become pregnant
  • Neurogenic or congenital disorders resulting in faecal incontinence (e.g. Multiple Sclerosis, uncontrolled diabetes, Parkinson's disease, Spina Bifida)
  • Inflammatory bowel disease
  • Chronic diarrhoea uncontrolled by medication or diet
  • Previous rectal surgery (rectopexy or rectal resection)

Sites / Locations

  • Chinese University of Hong Kong

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Sham Comparator

Arm Label

AcuTENS

Sham

Arm Description

Patients treated with TENS over Acupuncture points for faecal incontinence

Sham treatment arm with no electrical stimulations over acupuncture points

Outcomes

Primary Outcome Measures

Effectiveness of AcuTENS as treatment for faecal incontinence compared with sham intervention
Response to treatment is defined as 50% or greater change in Faecal incontinence Severity index score compared to sham

Secondary Outcome Measures

Changes in the severity of faecal incontience
Wexner score will be used the assess the severity of faecal incontinence
Episodes of faecal urgency per week
the number of episodes of faecal urgency experienced by the patient per week
Reduction in the number of incontinence episode per week
the number of episodes of faecal incontience experienced by the patient per week
Differences in Quality of Life score between two groups
using the tradition chinese version of the faecal incontinence quality of life questionnaire (FIQL)

Full Information

First Posted
February 2, 2021
Last Updated
February 6, 2021
Sponsor
Chinese University of Hong Kong
Collaborators
Health and Medical Research Fund
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1. Study Identification

Unique Protocol Identification Number
NCT04749316
Brief Title
Acs-Tens Treatment for Faecal Incontinence: a RCT With Sham-controls
Official Title
Transcutaneous Electric Nerve Stimulation on Acupoints (Acu-TENS) for the Treatment of Faecal Incontinence: a Prospective, Randomised, Sham-controlled Trial.
Study Type
Interventional

2. Study Status

Record Verification Date
February 2021
Overall Recruitment Status
Completed
Study Start Date
August 1, 2017 (Actual)
Primary Completion Date
October 30, 2020 (Actual)
Study Completion Date
December 31, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Chinese University of Hong Kong
Collaborators
Health and Medical Research Fund

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study assess the effectiveness on AcuTENS on the treatment of faecal incontinence
Detailed Description
Faecal incontinence (FI) is the involuntary loss of flatus, liquid or solid stool per rectum. Owing to the emotional stress and the psychosocial stigma surrounding this problem, it is under-reported by patients. Conservative management of FI involves lifestyle, medical adjustments and pelvic floor sphincter training. If conservative treatment fails, surgical options such as sphincter repair, sacral nerve stimulation (SNM) and percutaneous tibial nerve stimulation (PTNS) can be reformed. SNM and PTNS involve application of nervous electrical stimulation (neuromodulation) with significant improvement of symptoms. The positions of electrical stimuli are also very similar to acupuncture sites (acupoints) used in Traditional Chinese Medicine for the treatment of faecal incontinence. However, disadvantage of these methods are; 1) they are invasive and may cause complications such as pain, infection and bleeding and; 2) the devices for each SNM device can be costly. Transcutaneous Electrical Nerve Stimulation (TENS) is non-invasive, which is commonly used for the management of pain. It works via the application of electrical stimuli using adhesive gel pads. They are cheap to run and are widely accepted by patients. Hence application of TENS over acupoints (Acu-TENS) may provide a novel non-invasive treatment. A randomised controlled trial will be carried out on patients with FI. Demographic data, past medical history, in particular any structural or neurological causes of FI, will be recorded. Ano-rectal manometry and endoanal ultrasound will be performed before and after treatment. Acu-TENS machine will be applied to standardised acupuncture points. Assessment of FI via Cleveland Clinic Florida Faecal Incontinence Score and Quality of life measurements via the validated questionnaires Short Form 36 (SF-36) and the Fecal Incontinence Quality of Life Scale (FIQL) (Chinese version) questionnaires will be carried out at baseline, and followup intervals.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Faecal Incontinence, Faecal Incontinence With Faecal Urgency, Neuromodulation, Transcutaneous Electric Nerve Stimulation, Acupuncture Points
Keywords
Faecal incontinence, Faecal urgency, Neuromodulation, Transcutaneous Electric Nerve Stimulation, Acupuncture

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Acutens treatment for faecal incontinence vs sham
Masking
ParticipantOutcomes Assessor
Masking Description
participant will not be told on which treatment arm are in. Outcome assessors will be blinded on participants' treatment arm.
Allocation
Randomized
Enrollment
53 (Actual)

8. Arms, Groups, and Interventions

Arm Title
AcuTENS
Arm Type
Experimental
Arm Description
Patients treated with TENS over Acupuncture points for faecal incontinence
Arm Title
Sham
Arm Type
Sham Comparator
Arm Description
Sham treatment arm with no electrical stimulations over acupuncture points
Intervention Type
Procedure
Intervention Name(s)
AcuTENS
Intervention Description
Stimulation of acupuncture points with TENS machine
Primary Outcome Measure Information:
Title
Effectiveness of AcuTENS as treatment for faecal incontinence compared with sham intervention
Description
Response to treatment is defined as 50% or greater change in Faecal incontinence Severity index score compared to sham
Time Frame
post treatment 8 weeks and 6 months compared with baseline
Secondary Outcome Measure Information:
Title
Changes in the severity of faecal incontience
Description
Wexner score will be used the assess the severity of faecal incontinence
Time Frame
post treatment 8 weeks and 6 months compared with baseline
Title
Episodes of faecal urgency per week
Description
the number of episodes of faecal urgency experienced by the patient per week
Time Frame
post treatment 8 weeks and 6 months compared with baseline
Title
Reduction in the number of incontinence episode per week
Description
the number of episodes of faecal incontience experienced by the patient per week
Time Frame
post treatment 8 weeks and 6 months compared with baseline
Title
Differences in Quality of Life score between two groups
Description
using the tradition chinese version of the faecal incontinence quality of life questionnaire (FIQL)
Time Frame
post treatment 8 weeks and 6 months compared with baseline

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
99 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients aged 18 years or above Acupuncture naïve patients Faecal incontinence with solid or liquid stool causing disruption of lifestyle Psychological stability and suitability as determined by the investigator Failed conservative or surgical treatment Intact peripheral neurosensory nervous system as determined by clinical investigation Able to read and write Exclusion Criteria: Major internal and/or external sphincter defect (>120 degrees of sphincter circumference) Faecal impaction Presence of full thickness rectal prolapse Patients who have contact allergies to adhesive pads Implanted pacemaker, defibrillator, cardiopathy Pregnancy or intention to become pregnant Neurogenic or congenital disorders resulting in faecal incontinence (e.g. Multiple Sclerosis, uncontrolled diabetes, Parkinson's disease, Spina Bifida) Inflammatory bowel disease Chronic diarrhoea uncontrolled by medication or diet Previous rectal surgery (rectopexy or rectal resection)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Tony WC Mak, MD, FRCS
Organizational Affiliation
Chinese University of Hong Kong
Official's Role
Principal Investigator
Facility Information:
Facility Name
Chinese University of Hong Kong
City
Sha Tin
Country
Hong Kong

12. IPD Sharing Statement

Plan to Share IPD
No

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Acs-Tens Treatment for Faecal Incontinence: a RCT With Sham-controls

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