Fecal Incontinence Treatment (FIT) Study
Study Details
Study Description
Brief Summary
Patients with severe fecal incontinence (FI), defined as two or more episodes of staining, solid or liquid FI per week, and who meet the inclusion criteria for Injection of Solesta (INJ; an inert bulking agent), or Biofeedback (BIO) will be enrolled. The baseline rate of FI will be assessed using a 2-week daily stool diary. All participants will initially be enrolled into a 4-week trial of Enhanced Medical Management (EMM; education, pelvic floor exercises, and use of non-prescription drugs to normalize stool consistency). Those who demonstrate at least a 75% reduction in FI frequency will not be randomized to one of the two treatment groups but will be followed-up for two years. Those not showing a 75% reduction in FI frequency will be randomized to BIO or INJ and will be evaluated three months later with respect to efficacy for reducing the frequency of fecal incontinence, safety of the interventions, and cost of providing care. All participants who experience a 75% decrease in FI after three months of treatment, compared to baseline, will be followed-up for a further 21 months, for a total of 24 months from the time of treatment initiation. To assess the long-term response to treatment, those who improve less than 75% in FI episodes will be offered an additional treatment with either the treatment to which they were not randomized or sacral nerve stimulation (SNS). Anorectal manometry and Magnetic Evoked Potentials will be used to subtype the physiological basis for FI. Quality of life and psychological factors will be used to assess outcomes.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
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N/A |
Detailed Description
This is an unmasked, multisite, randomized, parallel group study comparing the effectiveness of two treatments [BIO and INJ] for moderate to severe FI:
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Baseline: Participants will keep a daily symptom diary for two weeks to (a) document that they meet the minimum frequency required for inclusion in the study and (b) provide a reference value for assessing treatment response at the end of EMM and at 3, 6, 12, and 24 months follow-up points.
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EMM: All participants meeting inclusion criteria will first be treated with EMM for 4 weeks. The key components of treatment are patient education about the basic physiological mechanisms for defecation, diet and medication to normalize stool consistency, and pelvic floor exercises taught by printed instructions. Additional goals of the EMM protocol are (a) to ensure that participants randomized to BIO or INJ meet the accepted criteria for these treatments by failing to respond to EMM, and (b) to document the efficacy and the durability of systematically applied, optimized EMM. Patients who are responders to EMM will be followed up 3 months later; those who remain responders will be continued on EMM and followed for the remaining 24 months of the study. However, those who are no longer responders to this conservative treatment after 3 months will be invited to be randomized to BIO or INJ and all outcome measures will be assessed at 3 months from initiation of the treatment arm to which they are randomized. They will be pooled with other patients randomly assigned to the same treatment for the primary analyses and will be assessed at 6 months.
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Randomly assigned treatment: Each participant who fails the EMM will be randomly assigned to BIO or INJ and treated as follows:
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BIO will consist of 5-6 one-hour training sessions spaced at weekly intervals. These will occur in the first 5-6 weeks of treatment. Treatment approaches will include strength training in all participants, sensory training for participants with hyposensitivity, and/or urge-resistance training for participants with hypersensitivity to the sensations caused by rectal distention. Home exercises will be assigned to participants to practice these skills, and these will be guided by a brochure.
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INJ will include a preparation for treatment and a treatment visit. The preparation will involve prophylactic antibiotics for the day of the procedure and minimal restrictions on food intake. On the day of the procedure, a physician will inject 1 ml of dextranomer into each of 4 quadrants of the rectum proximal to the dentate line. Ten seconds will be allowed to pass before the injection needle is withdrawn to minimize drainage of the dextranomer. The participant will be scheduled to return in 6 weeks for possible repeat injection of a second 4 ml of dextranomer. At this second appointment, if FI has improved by 75% or more compared to baseline, the participant will be continued without a second injection. However, if the rate of FI is greater than 75% of baseline, the participant will be offered a second injection of dextranomer.
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Combination therapy: The primary assessment of efficacy is at 3 months following the first treatment visit completed, and participants who have not achieved at least a 75% reduction in FI frequency compared to baseline will be classified as treatment failures; they will be invited to choose the treatment to which they were not randomized or SNS as an adjunctive treatment for the remaining months of the study. One reason for this is to increase the likelihood that participant will consent to be randomized despite possibly having a priori preferences for one of the two treatments. Thus, the participants who add a second treatment and continue to be monitored up to 24 months will constitute a pragmatic clinical trial (i.e., the study design for these participants going forward emulates the clinical situation in which patients who have an unsatisfactory response to a treatment are offered a new treatment or an ancillary treatment).
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Long-term follow-up: An intention-to-treat analysis of efficacy will be carried out at 6, 12 and 24 months. For these analyses, all participants randomized to treatment will be included in the analysis. All treatments will continue to be active. The bulking agents injected in the INJ treatment will remain in place. For BIO, participants will be encouraged to continue to practice pelvic floor exercises and enhanced awareness of rectal sensations following the initial training period. Participants who withdraw from the study or who fail treatment at 3 months will be evaluated as treatment failures in follow-up analyses of efficacy. Data will be collected from participants who add an alternative treatment at 3 months, but these data will not be considered in this analysis. Safety data will be collected at every visit. Participants who are responders at 3 months will continue to monitor symptoms for an additional 21 months (2 years total) whereas participants who are non-responders at 3 months will be retained as treatment failures in the long-term analysis of the comparative effectiveness of the BIO and INJ treatments. For longitudinal assessments of safety, cost, and secondary outcomes such as quality of life and FI severity scales, statistical models will include data from follow up time points through 24 months.
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Adjust for Expectation of Benefit: In a trial comparing behavioral and medical therapy, participants cannot be masked. The validated Credibility/Expectancy Questionnaire was developed to assess the patient's expectation of benefit after initial exposure to treatment and was used in previous studies to determine whether there is equipoise between the active and control conditions in behavioral treatment trials.
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Characterization of Enhanced Medical Treatment - Durability of improvement and predictors of response: The primary purpose of treating all participants with an EMM run-in is to be able to exclude participants who do not require more costly interventions. However, the investigators will take advantage of the opportunity provided by this run-in study to identify predictors of response to EMM and to assess the durability of improvements. EMM will not be "usual care" but will follow a written protocol that is intended to optimize EMM, which is why this is labelled enhanced medical management. Participants who are treatment responders at the end of the EMM run-in will be scheduled for 3-month follow-up, and those who are no longer treatment responders at 3 months follow-up will be offered an opportunity to be randomized to one of the 3 treatments at this point. However, those who remain responders to EMM at 3 months follow-up will continue to be followed for an additional 21 months. All participants, regardless of their outcomes at the end of EMM, will be encouraged to continue using the treatment approaches learned during the EMM phase.
Each participant will be studied for 24-27 months after completing the month of EMM and the anticipated duration of the study is 4.5 years from first enrollment to completion of the last participant. Approximately 285 adult participants, both male and female, will be recruited for EMM to ensure that 194 participants who did not benefit from EMM will be available for randomization to the two treatment arms (97 per treatment arm). The participants may be referred by clinicians or may respond to posted advertisements about the study.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Active Comparator: Biofeedback (BIO) Participants will receive biofeedback intervention during five (5) required weekly 1-hour sessions. A 6th treatment session will be made available for participants if it is shown through anorectal manometry that they are having trouble understanding directions given during the first five sessions. |
Behavioral: Biofeedback
The participant will learn how to improve strength and rectal sensation during five (5) - six (6) visits each lasting 60 minutes.
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| Active Comparator: Injection (INJ) Bulking agent injected into rectal wall to narrow opening. Two visits each lasting 45 minutes at weeks 0 and 6 respectively. |
Device: Injection
The participant will have a bulking agent injected into rectal wall to narrow opening. Two visits each lasting 45 minutes at weeks 0 and 6 respectively.
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Outcome Measures
Primary Outcome Measures
- Treatment Response Defined as a 75% or Greater Change in Number of Average Weekly FI Episodes at Month 3 Follow-Up Compared to Baseline [3-month follow-up]
FI episodes will be assessed using a validated symptom diary at Baseline and at three months follow-up.
- Proportion of Participants with Specified Adverse Events at Month 3 Follow-Up [3-month follow-up]
Adverse events of pelvic pain of grade II or higher based on Common Terminology Criteria for AE (CTCAE) criteria, treatment site infection, or serious adverse events (SAEs) requiring hospitalization.
- Treatment Costs at Month 3 Follow-Up [3-month follow-up]
Costs will be measured from three sources: (a) Number of treatment visits multiplied by the Medicare reimbursement rates. (b) An Out-of-Pocket Treatment Cost Questionnaire. (c) A Work Productivity and Impairment Questionnaire for direct and indirect costs. These costs will be combined to establish overall costs.
Secondary Outcome Measures
- Change in the Severity of FI as Assessed Using the Fecal Incontinence Severity Scale [up to 24 months]
Treatment effect on the severity of FI at 3-month follow-up, compared to baseline, will be assessed using the Fecal Incontinence Severity Scale, a validated FI severity scale which incorporates the frequency of different types of stool loss (solid, liquid, staining and a combination), the circumstances surrounding FI (urgency, passive, combined, or neither), and volume of leakage. Higher scores indicate more severe fecal incontinence. Assessed at Baseline, Months 6, 12, and 24.
- Change in Quality of Life as Assessed Using the Fecal Incontinence Quality of Life Scale [up to 24 months]
Treatment effect on the impact of FI on quality of life will be assessed using the Fecal Incontinence Quality of Life Scale which contains 29 items and is scored for four subscales: Lifestyle, Coping/Behavior, Depression/Self-Perception, and Embarrassment. Scores for each item range from 1 - 4 with 1 indicating a lower functional status of quality of life. Scale scores are the average (mean) response to all items after adjusting for missing and not applicable items. Assessed at Baseline, Months 6, 12, and 24.
- Change in Psychological Distress as Assessed Using the 7-item Patient-Reported Outcomes Measurement Information System (PROMIS) Anxiety Scale [up to 24 months]
One of the measures of psychological distress is the 7-item PROMIS Anxiety Scale for which higher scores indicate higher levels of anxiety. The Anxiety Scale (SF 7a) has a score range of 5 - 35. Assessed at Baseline, Months 6, 12, and 24.
- Change in Psychological Distress as Assessed Using the 8-item PROMIS Depression Scale [up to 24 months]
One of the measures of psychological distress is the 8-item PROMIS Depression Scale for which higher scores indicate higher levels of depression. The Depression Scale (SF 8a) has a score range of 5 - 40. Assessed at Baseline, Months 6, 12, and 24.
- Change in Psychological Distress as Assessed Using the 8-item PROMIS Self-Efficacy Symptom Management Scale [up to 24 months]
One of the measures of psychological distress is the 8-item PROMIS Self-Efficacy Symptom Management Scale for which higher scores indicate higher levels of self-efficacy. The Self-Efficacy for Managing Symptoms Scale (SF 8a) has a score range of 5 - 40. Assessed at Baseline, Months 6, 12, and 24.
- Number of Participants with Reduction of 50% or More in Average Weekly FI Episodes [up to 24 months]
Assessed at Baseline, Months 6, 12, and 24.
- Proportion of Participants Who are Continent [up to 24 months]
Assessed at Baseline, Months 6, 12, and 24.
Eligibility Criteria
Criteria
Inclusion Criteria:
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Physician diagnosis of FI (R15) for the past 6 months or longer.
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Able to ambulate independently on level surfaces. Patient may use assistive devices other than parallel bars.
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Average >2 staining, solid or liquid FI episodes per week by self-report and during the two-week baseline
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Meets criteria for dextranomer treatment except an internal anal sphincter defect of 180 degrees or less is acceptable.
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Less than 75% reduction in the number of FI episodes after 4 weeks of conservative treatment.
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Age >=18 years
Exclusion Criteria:
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Dementia, assessed using the Six-Item Screener to Identify Cognitive Impairment.
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Obstetrical injuries including third and fourth degree tears in the anal sphincter within the past 6 months.
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Pregnant or planning pregnancy in next 2 years
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Internal anal sphincter separation >180 degrees on ultrasound or magnetic resonance imaging
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Spinal cord injury or spina bifida
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Congenital malformation of anus or rectum
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Complete rectal prolapse or grade III/IV hemorrhoids
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History of previous anorectal surgery, such as stapled transanal rectal resection (STARR). Stapled hemorrhoidectomy is not an exclusion if performed more than 12 months previously. The FENIX® procedure, artificial anal sphincter or transposed gracilis; surgical hemorrhoidectomy (other than stapled), sphincteroplasty, rectal reconstructions and ileoanal pouches are permitted if performed more than 6 months previously and the patient meets inclusion criteria.
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Established diagnosis of inflammatory bowel disease
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Intestinal stoma present
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History of pelvic radiation within previous 12 months or presence of active radiation proctitis.
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Patients who cannot expel the rectal balloon during the balloon expulsion test and who have constipation most of the time.
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Anatomic limitations to placement of dextranomer injections.
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Presence of existing implant in the anal or rectal region
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Allergy to hyaluronic acid-based products
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Active anal or rectal conditions in the last 6 months including abscess, fissures, sepsis, significant bleeding, proctitis, colovaginal and rectovaginal fistulas, anal or rectal tumors, or other infections.
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The patient's physician believes it is unsafe for the patient to temporarily stop anticoagulants for any test procedures and treatments associated with the study.
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Patients who have 4 or more days with 4 or more bowel movements classed as a 6 or 7 on the Bristol Stool Scale per day in either (any) week bowel movements classed as a 6 or 7 during the Baseline will be excluded.
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Patients with Parkinson's disease, multiple sclerosis, severe diabetic neuropathy documented by electromyography (EMG), and neurodegenerative disorder.
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Patients currently receiving immunotherapy or chemotherapy.
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Significant anal pain in the last 6 months.
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Unwillingness of participant to stop using over-the-counter medications, herbal supplements, or prescribed medications for the purpose of modifying stool consistency, that are not included in the approved medications list (loperamide, laxatives, fiber supplements, and Questran are approved medications), for the duration of the research study.
Medical history will be documented to test for predictors of response.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | University of Alabama at Birmingham | Birmingham | Alabama | United States | 35801 |
| 2 | Augusta University Medical College of Georgia | Augusta | Georgia | United States | 30912 |
| 3 | University of Michigan | Ann Arbor | Michigan | United States | 48109 |
| 4 | Mayo Clinic | Rochester | Minnesota | United States | 55905 |
| 5 | Colon and Rectal Surgery Associates, Ltd. | Saint Paul | Minnesota | United States | 55114 |
| 6 | The University of North Carolina at Chapel Hill | Chapel Hill | North Carolina | United States | 27599 |
Sponsors and Collaborators
- University of North Carolina, Chapel Hill
- National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
- Mayo Clinic
- Colon and Rectal Surgery Associates, Ltd.
- Augusta University
- RTI International
Investigators
- Principal Investigator: William Whitehead, PhD, University of North Carolina, Chapel Hill
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- 17-0525
- 1U01DK115575-01