Controlling Anal Incontinence by Performing Anal Exercises With Biofeedback or Loperamide (CAPABLe)

This study is currently recruiting participants. (see Contacts and Locations)
Verified June 2014 by NICHD Pelvic Floor Disorders Network
Sponsor:
Collaborators:
The Cleveland Clinic
University of Alabama at Birmingham
University of California, San Diego
Duke University
University of New Mexico
Women and Infants Hospital of Rhode Island
RTI International
University of Pennsylvania
University of Pittsburgh
Information provided by (Responsible Party):
NICHD Pelvic Floor Disorders Network
ClinicalTrials.gov Identifier:
NCT02008565
First received: December 6, 2013
Last updated: June 12, 2014
Last verified: June 2014
  Purpose

The goals of this trial are to compare the use of loperamide to oral placebo and to compare the use of anal sphincter exercise training with biofeedback to usual care (educational pamphlet) in the treatment of women suffering from fecal incontinence (FI). We will test the following null hypotheses:

  1. there is no difference in outcomes between women randomized to loperamide and women randomized to oral placebo for treatment of FI;
  2. there is no difference in outcomes between women randomized to anal sphincter exercises with biofeedback and women randomized to usual care (educational pamphlet) for FI treatment;
  3. there is no difference between women randomized to both treatments together and women randomized to either FI treatment alone; and
  4. there is no correlation between anal manometry measurements and digital anal squeeze strength or measures of FI severity and bother.

Condition Intervention Phase
Fecal Incontinence
Drug: Loperamide
Drug: Placebo
Behavioral: Anal exercises with biofeedback
Behavioral: Usual Care
Phase 3

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Factorial Assignment
Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor)
Primary Purpose: Treatment
Official Title: Controlling Anal Incontinence by Performing Anal Exercises With Biofeedback or Loperamide (CAPABLe): a Randomized Placebo Controlled Trial

Resource links provided by NLM:


Further study details as provided by NICHD Pelvic Floor Disorders Network:

Primary Outcome Measures:
  • Change from baseline St. Mark's (Vaizey) Score [ Time Frame: 24 week visit ] [ Designated as safety issue: No ]
    The primary outcome measure for all study arms is the change from baseline in St. Mark's (Vaizey) Score 24 weeks after treatment initiation to compare the marginal outcomes of anal exercise with biofeedback to usual care and loperamide to placebo.


Secondary Outcome Measures:
  • Condition-specific and generalized quality of life [ Time Frame: 12 and 24 week visits ] [ Designated as safety issue: No ]
    Change in quality of life between those randomized to loperamide compared to placebo and between those randomized to anal sphincter exercises with biofeedback compared to usual care (educational pamphlet).

  • Efficacy Measures [ Time Frame: 12 and 24 week visits ] [ Designated as safety issue: No ]
    Measures of efficacy include bowel diary measures, digital rectal tone, and anal manometry measures .

  • Patient satisfaction [ Time Frame: 12 and 24 week visits ] [ Designated as safety issue: No ]
    Participants' satisfaction with FI treatment modality defined as a response that their condition is "much better" or "very much better" on the PGI-I.

  • Cost-effectiveness of FI treatment [ Time Frame: 12 and 24 week visits ] [ Designated as safety issue: No ]
    Cos-effectiveness of FI treatment modalities will be assessed using the patient's and societal perspectives.

  • Succes of masking the drug treatment arm [ Time Frame: 24 week visit ] [ Designated as safety issue: No ]
    The purpose of this outcome is to assess the extent to which masking of the drug treatment arm is successful with respect to both the patient and the study coordinator.


Estimated Enrollment: 294
Study Start Date: February 2014
Estimated Study Completion Date: September 2016
Estimated Primary Completion Date: February 2016 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Placebo Comparator: Placebo Drug: Placebo
Participants randomized to the placebo arm will begin the a dose of one capsule per day and will be dose increased or dose decreased using the same algorithm described for the loperamide arm.
Experimental: Anal exercises with biofeedback Behavioral: Anal exercises with biofeedback
Subjects randomized to anal exercises with biofeedback will receive a formal anal exercises training program designed by experts in the use of manometry and biofeedback for fecal incontinence. The intent is to provide a simple program that can be easily applied in an office setting with minimal subject burden. Subjects will attend six separate anal exercises with biofeedback sessions with trained personnel over a 12-week period for the 24-week study. Sessions will include introduction, standard patient education, and exercises using anal manometry-assisted biofeedback introducing concepts such as shaping, generalization and termination. The protocol will include strength and sensory training including urge resistance training. During the final twelve weeks, subjects will perform anal exercises on their own. The sessions with interventionists will occur every other week for 12 weeks (total 6 supervised sessions).
Placebo Comparator: Usual care Behavioral: Usual Care
Usual care consists of patients receiving an educational pamphlet on fecal incontinence created by the National Institute of Diabetes and Digestive and Kidney Diseases.
Experimental: Loperamide Drug: Loperamide
Participants randomized to the loperamide treatment group will begin with 2mg of loperamide per day. The participant will be administered the Patient Global Symptom Control rating scale (PGSC) to determine dose escalation. The participant will be instructed to either maintain the current drug dose if PGSC is 4 or 5, or dose escalate if PGSC is 1-3. Participants who report inadequate control of stool leakage on the PGSC will be instructed to increase the daily dose of loperamide by 2 mg up to a maximum of 8 mg per day (1-4 capsules). Bothersome adverse events and resulting dose reduction will be based exclusively on the result of the PGTS. The participant will be instructed to reduce the current drug dose if PGTS is 4 or 5. The daily dose will be decreased by 2mg to a minimum of 2mg every other day. If they have a PGSC score of 1-3 (inadequate control of stool leakage) combined with a PGTS score of 4-5 (bothersome side effects), the participant will discontinue the study medication.
Other Name: Imodium

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Female
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Age ≥18 years
  • Fecal incontinence defined as any uncontrolled loss of liquid or solid fecal material that occurs at least monthly over the last 3 months that is bothersome enough to desire treatment

Exclusion Criteria:

  • Stool consistency over the last 3 months that includes items 1 or 7 based on the Bristol Stool form scale
  • Current or past diagnosis of colorectal or anal malignancy
  • Diagnosis of inflammatory bowel disease
  • Current or history of rectovaginal fistula or cloacal defect
  • Rectal prolapse (mucosal or full thickness)
  • Prior removal or diversion of any portion of colon or rectum
  • Prior pelvic floor or abdominal radiation
  • Refusal or inability to provide written consent
  • Inability to conduct telephone interviews conducted in English or Spanish
  • Fecal impaction by exam
  • Untreated pelvic organ prolapse beyond the hymen; Patients with prolapse beyond the hymen who are currently using a pessary are eligible
  • Incontinence only to flatus
  • Has taken any loperamide (Imodium®) or diphenoxylate plus atropine (Lomotil®) in the last 30 days
  • Previously received and failed treatment of fecal incontinence using loperamide (Imodium®) or diphenoxylate plus atropine (Lomotil®) over the last 3 months
  • Current supervised anal sphincter exercise/pelvic floor muscle training with biofeedback
  • Previously received and failed treatment of fecal incontinence using supervised anal sphincter exercise/pelvic floor muscle training with biofeedback
  • Previous allergy or intolerance to loperamide
  • Pregnant, nursing, or planning to become pregnant before the end of the study follow-up period.
  • Childbirth within the last 3 months
  • Currently taking anti-retroviral drugs
  • Neurological disorders known to affect continence, including spinal cord injury, advanced multiple sclerosis or Parkinson's disease and debilitating stroke
  • Known diagnosis of hepatic impairment
  • Chronic abdominal pain in the absence of diarrhea
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT02008565

Contacts
Contact: J E Jelovsek, MD jelovsj@ccf.org
Contact: Susan Meikle, MD

Locations
United States, Alabama
University of Alabama at Birmingham Recruiting
Birmingham, Alabama, United States, 35233
Contact: Velria Willis       vwillis@uabmc.edu   
Principal Investigator: Alayne Markland, DO, MSc         
United States, California
University of California at San Diego Recruiting
La Jolla, California, United States, 92037-0974
Contact: JoAnn Columbo       jcolumbo@ucsd.edu   
Principal Investigator: Charles W Nager, MD         
Kaiser San Diego Recruiting
San Diego, California, United States, 92110
Contact: Gisselle Zazueta- Damian       Gisselle.Zazueta-Damian@kp.org   
Contact: Linda Mackinnon       Linda.m.mackinnon@kp.org   
Principal Investigator: Keisha Dyer         
United States, New Mexico
University of New Mexico Recruiting
Albuquerque, New Mexico, United States, 87131
Contact: Susan Lee       srlee@salud.unm.edu   
Contact: Elizabeth Hervey       ECHervey@salud.unm.edu   
Principal Investigator: Rebecca Rogers, MD         
United States, North Carolina
Duke University Recruiting
Durham, North Carolina, United States, 27707
Contact: Mary Raynor       mary.raynor@duke.edu   
Principal Investigator: Anthony G Visco, MD         
United States, Ohio
Cleveland Clinic Recruiting
Cleveland, Ohio, United States, 44195
Contact: Ly Pung       pungl@ccf.org   
Contact: Geetha Krishna       KRISHNG@ccf.org   
Principal Investigator: Matthew Barber, MD         
Sub-Investigator: J E Jelovsek, MD         
United States, Pennsylvania
University of Pennsylvania Recruiting
Philadelphia, Pennsylvania, United States, 19118
Contact: Michelle Kinglee       kingleem@uphs.upenn.edu   
Principal Investigator: Diane Newman         
University of Pittsburgh Recruiting
Pittsburgh, Pennsylvania, United States, 15213
Contact: Judy Gruss       jgruss@mail.magee.edu   
Principal Investigator: Gary Sutkin, MD         
United States, Rhode Island
Brown/Women and Infants Hospital of Rhode Island Recruiting
Providence, Rhode Island, United States, 02903
Contact: Ann Meers       ameers@wihri.org   
Principal Investigator: Vivian Sung, MD         
Sponsors and Collaborators
NICHD Pelvic Floor Disorders Network
The Cleveland Clinic
University of Alabama at Birmingham
University of California, San Diego
Duke University
University of New Mexico
Women and Infants Hospital of Rhode Island
RTI International
University of Pennsylvania
University of Pittsburgh
Investigators
Study Chair: J E Jelovsek The Cleveland Clinic
Study Chair: Matthew Barber The Cleveland Clinic
  More Information

No publications provided

Responsible Party: NICHD Pelvic Floor Disorders Network
ClinicalTrials.gov Identifier: NCT02008565     History of Changes
Other Study ID Numbers: PFDN- 18PO1, 2U10HD041261, 2U10HD054215, 2U10HD041267, 1U10HD069006, 2U10HD054214, 1U10HD069013, 1U10HD069025, 1U10HD069010, 1U01HD069031
Study First Received: December 6, 2013
Last Updated: June 12, 2014
Health Authority: United States: Food and Drug Administration

Keywords provided by NICHD Pelvic Floor Disorders Network:
Fecal incontinence
Loperamide
anal exercises
biofeedback

Additional relevant MeSH terms:
Fecal Incontinence
Rectal Diseases
Intestinal Diseases
Gastrointestinal Diseases
Digestive System Diseases
Loperamide
Antidiarrheals
Gastrointestinal Agents
Therapeutic Uses
Pharmacologic Actions

ClinicalTrials.gov processed this record on September 18, 2014