Efficacy of Psychological Therapies in Patients With Functional Bowel Disorders

Constipation Clinical Trial

— PTSD  

Official title:

Efficacy of Psychological Therapies in Patients With Functional Bowel Disorders With History of Early Adverse Life Events or Post-traumatic Stress Disorder

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04060121
• Other study ID #: 1802270023
• Secondary ID: UL1TR002529
• Status: Completed
• Start date: June 1, 2018
• Est. completion date: November 29, 2022

Study information

• Verified date: April 2024
• Source: Indiana University
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

The purpose of this study is study bowel symptoms, quality of life, and personal factors that may affect your health. In Aim 1 of this study participants will be invited to complete 6 survey-based questionnaires online. In Aim 2 of this study will monitor the effectiveness of a 12 week therapy program on bowel symptoms and overall quality of life.

Description:

For Aim 1, investigators will conduct a cross-sectional survey study examining prevalence of early adverse life events and post-traumatic stress disorder (PTSD) in patients with constipation-predominant IBS or chronic constipation with or without overlapping dyssynergic defecation. For Aim 2, investigators will recruit and enroll individuals who have a positive history of early adverse life events or possible PTSD as identified in Aim 1 for a 12 week outpatient cognitive behavioral therapy program as outlined below: Visit 1 (Participants will present to the GI Office at one of our dedicated locations including the downtown Digestive and Liver Disorders (DaLD) clinic, Springmill Clinic, or IU North Multispeciality Clinic) At this screening visit, participants do the following: - Read and sign the informed consent after all your questions about the study will be answered - Have a medical history taken including demographics, symptoms and history of illness - Medications will be reviewed - A physical exam will be performed by the physician if the visit is being conducted in person. If the visit is done virtually, the physician will record that exam as a virtual exam with all relevant information that can be gathered by a virtual exam. - Vital signs will be measured if the visit is conducted in person. If the visit is virtual, vital signs will not be physically done but any available data pertaining to vital signs will be documented. - Participants will be asked to complete a series of questionnaires - Participants will be provided a bowel pattern diary to record bowel symptoms over the course of the study - Participants will be asked to complete global assessment scales (2 questions) during each week of the study - Participants will be administered the PAC-SYM, PAC-QOL, global assessment scale, SF-12, HADS and PCL-5 during CBT - Participants will be administered the GAD-7 and PHQ-9 at every CBT visit. - The study visit may take 30 minutes to 1 hour to complete Day 1-15 (Run-In Phase): • Participants be asked to record stool symptoms and patterns in a diary daily starting from Day 1 to Day 15. The daily dairy can either be completed on paper or by phone or on the web. Day 16-100 (Visit 2-13): During this time, participants will undergo regular sessions with a dedicated GI psychologist. They will receive one 60-minute session every week for 10-12 weeks. The treatment schedule will include education on the relationship between bowel symptoms and stressful life events with instructions on ways to cope and manage symptoms through the use of relaxation techniques, such as breathing exercises and other methods for self calming. During the 10 to 12 weeks of therapy, participants will be given assignments and asked to monitor your progress. After you have completed your treatment sessions, you will be asked to fill out the same questionnaires that you completed at your screening visit that can be done either in person using a physical form or virtually online. Visit 14: • We will also confirm completion of the study.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 126
• Est. completion date: November 29, 2022
• Est. primary completion date: November 29, 2022
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

Aim 1:

-Patients with a history of constipation based on clinical evaluation undergoing diagnostic testing for dyssynergic defecation with anorectal manometry with balloon expulsion test, ages 18 years or older.

Aim 2:

• Patients with a history of constipation with or without dyssernergic defecation and a positive history of EALs or PTSD, as identified in Aim 1 based on survey responses.
• Any positive history regardless of symptom severity will be considered. Positive history will be defined by an ACE score of 1 or higher OR a provisional diagnosis of PTSD. A provisional PTSD diagnosis can be made by treating each PCL-5 item rated as 2 = "Moderately" or higher as a symptom endorsed. The diagnostic rule will require a rating of "moderate" for the following: 1 B item (questions 1-5), 1 C item (questions 6-7), 2 D items (questions 8-14), and 2 E items (questions 15-20). Exclusion Criteria:

For Aim 1, key exclusion criteria are:

• Patients who are currently hospitalized
• Patients who are unable to consent
• Patients with microscopic colitis, inflammatory bowel disease, or celiac disease, visceral cancer, or uncontrolled thyroid disease. In Aim 2, key exclusion criteria will include the aforementioned criteria listed in Aim 1

as well as the following:

• Patients who have bipolar disorder including active or recent hypomanic/manic episode
• Patients at imminent risk for harm to self or others
• Patients unable to follow orders
• Patients who have a history of organic brain disease
• Patient using illicit substances
• Pregnant or post-partum patients
• Patients who are homeless or lacking sufficient social support for follow-up care
• Patients with acute stress disorder as determined by the GI psychologist
• Patients with or severe PTSD as determined by the GI psychologist

Related Conditions & MeSH terms

• Constipation
• IBS - Irritable Bowel Syndrome
• Intestinal Diseases
• Irritable Bowel Syndrome

Locations

Country	Name	City	State
United States	Indiana University School of medicine	Indianapolis	Indiana

Sponsors (4)

Lead Sponsor	Collaborator
Indiana University	Indiana Clinical and Translational Sciences Institute, Indiana University Health, National Center for Advancing Translational Sciences (NCATS)

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Early adverse life events (EALS)	Presence of early adverse life events will be determine by self-reported questionnaire responses to the adverse childhood experiences (ACE) questionnaire (ACE score of one or higher, range 0-8)	10-15 minutes
Primary	Post-traumatic Stress Disorder (PTSD)	Prevalence of PTSD will be determined by self-reported questionnaire responses to PTSD Checklist (PCL-5) questionnaire (range 0-80). A provisional PTSD diagnosis can be made by treating each item rated as 2 = "Moderately" or higher as a symptom endorsed, then following the DSM-5 diagnostic rule which requires at least: 1 B item (questions 1-5), 1 C item (questions 6-7), 2 D items (questions 8-14), 2 E items (questions 15-20).	10-15 minutes
Primary	Change in weekly number of complete spontaneous bowel movements	The weekly number of complete spontaneous bowel movements will be measured using a validated daily bowel diary	12 weeks
Primary	Change in abdominal pain	Abdominal pain will be measured using a validated daily bowel diary	12 weeks
Secondary	IBS or functional constipation (FC)	Presence of IBS or FC will be determined based on responses to the validated IBS Rome IV Questionnaire	20-30 minutes
Secondary	Psychological comorbidities	Existence and severity of psychological comorbidities will be measured by the validated hospital anxiety and depression scale (HADS) questionnaire (range 0-14)	20-30 minutes
Secondary	Health-related quality of life: Short Form-12 (SF-12)	Health-related quality of life will be measured by responses to SF-12 (higher score is better, range 0-100)	20-30 minutes
Secondary	Constipation-related symptoms	Change in constipation-related symptoms will be measured using the validated in Patient Assessment of Constipation Symptoms questionnaire (higher score is worse, score range 0-4)	12 weeks
Secondary	Constipation-related quality of life	Change in constipation-related quality of life will be measured using the validated patient assessement of constipation quality of life questionnaire (higher score is worse, score range 0-4)	12 weeks