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The Use of an "Anal-Tape" in Patients With Fecal Incontinence

Primary Purpose

Fecal Incontinence

Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Anal Tape
Sponsored by
Shaare Zedek Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Fecal Incontinence

Eligibility Criteria

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

Inclusion Criteria:

  • >18 years old
  • Fecal incontinence for more than 6 months
  • Willing to participate
  • Understand the study procedures
  • Is able to apply and remove the "anal tape" without significant assistance of others.
  • Have done sigmoidsocopy or colonoscopy and anal manometry within five year of screening visit

Exclusion Criteria:

  • Advanced full thickness rectal prolapse.
  • Injured, inflamed or any significant disease in the peri-anal skin.
  • Allergy to any component of the device, either known or developed during testing in the screening visit.
  • Moderate to severe proctitis of any etiology.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    No Intervention

    Experimental

    Arm Label

    Off treatment

    Treatment period

    Arm Description

    2 week period without intervention

    2 week period with intervention

    Outcomes

    Primary Outcome Measures

    Any Improvment in the Fecal Incontince Quality of Life Scale (FIQoLs)
    The FIQoL is a validated, condition-specific tool that evaluates quality of life (QoL) in patients with fecal incontinence (FI) it consisting of 29 questions, subdivided into four domains: Lifestyle, Coping/Behavior, Depression/Self-perception, and Embarrassment. Item 1, general health, is graded from 1 "excellent" to 5 "poor" and is reversely scored. Items 2 to 28 are graded on a 4-point Likert-scale (1 = lower QoL). Item 29, FI specific depression, is graded from 1 "extremely so" to 6 "not at all." The average score for each domain is calculated separately and is calculated only if half or more of the items in the particular domain have been answered. Scales range from 1 to 5, with a 1 indicating a lower quality of life. Each domain or subscale is reported separately (Range 1 to 5), a total score including all four domains is not calculated.

    Secondary Outcome Measures

    A 50% Reduction in the Number of Episodes of FI Per Week
    Number of pateints with reduction of more than 50% in the absolute number of FI events during each week of the study
    Mean Wexner Score
    The Wexner Scale is a measure of frequency and severity of anal incontinence. It comprises five items, three regarding frequency of involuntary passage of gas, liquid, or solid stool, frequency of pad wearing, and frequency of lifestyle alteration, scored in a 5-point Likert-scale (never=0, rarely=1, sometimes=2, usually=3, always=4). A sum of all scores from 0 to 20 is calculated with higher scores meaning more severe incontince.
    Mean Redction in Wexner Scale Compared to Baseline
    The Wexner Scale is a measure of frequency and severity of anal incontinence. It comprises five items, three regarding frequency of involuntary passage of gas, liquid, or solid stool, frequency of pad wearing, and frequency of lifestyle alteration, scored in a 5-point Likert-scale (never=0, rarely=1, sometimes=2, usually=3, always=4). A sum of all scores from 0 to 20 is calculated with higher scores meaning more severe incontince.
    General Satisfaction
    General satisfaction with the device was assessed using a standard 100 mm visual analog scale. Patients were asked to grade their satisfaction with the device between 0 and 100 by drawing a perpendicular line in the 100 mm visual analog scale. Then the distance in mm was measured in mm from 0 to the perpendicular line and the score was calculated. Higher scores meaning better satisfaction.
    Willingness of the Patient to Continue Using the Anal Tape After the Study.
    Willingness of the patient to continue using the device was assessed using a standard 100 mm visual analog scale. Patients were asked to grade their willingness to use the device in the future between 0 and 100 by drawing a perpendicular line in the 100 mm visual analog scale. Then the distance in mm was measured in mm from 0 to the perpendicular line and the score was calculated. Higher scores meaning better satisfaction.

    Full Information

    First Posted
    December 7, 2016
    Last Updated
    April 1, 2020
    Sponsor
    Shaare Zedek Medical Center
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02989545
    Brief Title
    The Use of an "Anal-Tape" in Patients With Fecal Incontinence
    Official Title
    The Use of an "Anal-Tape" in Patients With Fecal Incontinence
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    April 2020
    Overall Recruitment Status
    Completed
    Study Start Date
    December 2016 (undefined)
    Primary Completion Date
    December 2018 (Actual)
    Study Completion Date
    December 2018 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Shaare Zedek Medical Center

    4. Oversight

    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    Fecal incontinence (FI), defined as the involuntary passage of stool for more than 3 months and is a devastating disease. The negative impact on quality of life has been consistently demonstrated. The prevalence of FI is probably underestimated in most studies. Currently conservative treatment is only modestly effective and surgical treatment is complex and expensive with less than optimal efficacy. The investigators developed an "anal tape" using a commercially available elastic band with a special adhesive that is approved for use in the skin. A special design of the tape can be applied to the skin surrounding the anus providing support and additional pressure forces to the anal sphincter. This is a 4 week, prospective, non blinded, cross-over study to explore the efficacy and safety of this device in patients with FI. The primary endpoint will be improvement in quality of life.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Fecal Incontinence

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Crossover Assignment
    Masking
    None (Open Label)
    Allocation
    Non-Randomized
    Enrollment
    20 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Off treatment
    Arm Type
    No Intervention
    Arm Description
    2 week period without intervention
    Arm Title
    Treatment period
    Arm Type
    Experimental
    Arm Description
    2 week period with intervention
    Intervention Type
    Device
    Intervention Name(s)
    Anal Tape
    Primary Outcome Measure Information:
    Title
    Any Improvment in the Fecal Incontince Quality of Life Scale (FIQoLs)
    Description
    The FIQoL is a validated, condition-specific tool that evaluates quality of life (QoL) in patients with fecal incontinence (FI) it consisting of 29 questions, subdivided into four domains: Lifestyle, Coping/Behavior, Depression/Self-perception, and Embarrassment. Item 1, general health, is graded from 1 "excellent" to 5 "poor" and is reversely scored. Items 2 to 28 are graded on a 4-point Likert-scale (1 = lower QoL). Item 29, FI specific depression, is graded from 1 "extremely so" to 6 "not at all." The average score for each domain is calculated separately and is calculated only if half or more of the items in the particular domain have been answered. Scales range from 1 to 5, with a 1 indicating a lower quality of life. Each domain or subscale is reported separately (Range 1 to 5), a total score including all four domains is not calculated.
    Time Frame
    2 weeks
    Secondary Outcome Measure Information:
    Title
    A 50% Reduction in the Number of Episodes of FI Per Week
    Description
    Number of pateints with reduction of more than 50% in the absolute number of FI events during each week of the study
    Time Frame
    4 weeks
    Title
    Mean Wexner Score
    Description
    The Wexner Scale is a measure of frequency and severity of anal incontinence. It comprises five items, three regarding frequency of involuntary passage of gas, liquid, or solid stool, frequency of pad wearing, and frequency of lifestyle alteration, scored in a 5-point Likert-scale (never=0, rarely=1, sometimes=2, usually=3, always=4). A sum of all scores from 0 to 20 is calculated with higher scores meaning more severe incontince.
    Time Frame
    2 weeks
    Title
    Mean Redction in Wexner Scale Compared to Baseline
    Description
    The Wexner Scale is a measure of frequency and severity of anal incontinence. It comprises five items, three regarding frequency of involuntary passage of gas, liquid, or solid stool, frequency of pad wearing, and frequency of lifestyle alteration, scored in a 5-point Likert-scale (never=0, rarely=1, sometimes=2, usually=3, always=4). A sum of all scores from 0 to 20 is calculated with higher scores meaning more severe incontince.
    Time Frame
    2 weeks
    Title
    General Satisfaction
    Description
    General satisfaction with the device was assessed using a standard 100 mm visual analog scale. Patients were asked to grade their satisfaction with the device between 0 and 100 by drawing a perpendicular line in the 100 mm visual analog scale. Then the distance in mm was measured in mm from 0 to the perpendicular line and the score was calculated. Higher scores meaning better satisfaction.
    Time Frame
    2 weeks
    Title
    Willingness of the Patient to Continue Using the Anal Tape After the Study.
    Description
    Willingness of the patient to continue using the device was assessed using a standard 100 mm visual analog scale. Patients were asked to grade their willingness to use the device in the future between 0 and 100 by drawing a perpendicular line in the 100 mm visual analog scale. Then the distance in mm was measured in mm from 0 to the perpendicular line and the score was calculated. Higher scores meaning better satisfaction.
    Time Frame
    4 weeks

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: >18 years old Fecal incontinence for more than 6 months Willing to participate Understand the study procedures Is able to apply and remove the "anal tape" without significant assistance of others. Have done sigmoidsocopy or colonoscopy and anal manometry within five year of screening visit Exclusion Criteria: Advanced full thickness rectal prolapse. Injured, inflamed or any significant disease in the peri-anal skin. Allergy to any component of the device, either known or developed during testing in the screening visit. Moderate to severe proctitis of any etiology.

    12. IPD Sharing Statement

    Citations:
    PubMed Identifier
    35039916
    Citation
    Livovsky DM, Koslowsky B, Goldin E, Lysy J. External kinesiology tape for improvement in fecal incontinence symptom bother in women: a pilot study. Int Urogynecol J. 2022 Oct;33(10):2859-2868. doi: 10.1007/s00192-021-05050-z. Epub 2022 Jan 18.
    Results Reference
    derived

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    The Use of an "Anal-Tape" in Patients With Fecal Incontinence

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