Irritable Bowel Syndrome
Conditions
Keywords
IBS, Relaxation, Emotional exposure, Emotional Processing
Brief summary
The primary goal of this study is to test the efficacy of emotional awareness and expression training (EAET), a novel emotional processing intervention that the investigators have developed, for people with IBS. In this randomized, controlled trial, the investigators will compare EAET to a standard intervention that teaches the conceptually opposite approach-relaxation training (RT)-and test how both of these interventions compare to a wait-list control condition. The investigators hypothesize that individuals in the EAET group will demonstrate greater improvement in their IBS symptom severity, psychological functioning, quality of life, and health care utilization at 4 and 12-week follow-up time points, compared to individuals in the wait-list control group. It is also expected that both of the active interventions (EAET and RT) will be more efficacious than the wait-list control condition.
Interventions
BEHAVIORALEmotional Awareness and Expression Training
An emotional processing intervention, which aims to reduce stress by helping patients become aware of, and express emotions related to stressful life experiences, as well as teaching patients how to relate to others differently.
BEHAVIORALRelaxation Training
Teaches patients different relaxation training skills to reduce their distress and discomfort (i.e., progressive muscle relaxation, applied relaxation, or guided imagery.
Sponsors
Wayne State University
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No
Inclusion criteria
To be eligible to participate, individuals must meet the Rome III criteria for IBS. That is, they must report that they have had: * recurrent abdominal pain or discomfort, or * a change in stool frequency or form, * at least three days per month, in the last three months, and * that they have been given this diagnosis by a physician. They must also report having pain and discomfort of at least two days per week at time of screening.
Exclusion criteria
* Individuals who report having post-infectious IBS, * organic gastrointestinal diseases (e.g., inflammatory bowel disease), immunodeficiency, * a current psychotic disorder, * drug or alcohol dependence within the past two years, and * those who are unable to communicate in English will be excluded.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| IBS symptom severity scale (IBS-SSS) | Change from baseline symptom severity at 1 month and 3 months |
Secondary
| Measure | Time frame |
|---|---|
| Ambivalence over Emotional Expression Scale (AEQ) | Change from baseline ambivalence over emotional expression at 1 month and 3 months |
| Positive and Negative Affect Scale (PANAS) | Change from baseline positive affect and negative affect at 1 month and 3 months |
| Impact of Events Scale - Revised (IES-R) | Change from baseline impact of events at 1 month and 3 months |
| Toronto Alexithymia Scale -20 (TAS-20) | Change from baseline alexithymia at 1 month and 3 months |
| McGill Pain Questionnaire, Short Form (SF-MPQ-2) | Change from baseline pain at 1 month and 3 months |
| Bristol Stool Form Scale (BSFS) | Change from baseline stool form at 1 month and 3 months |
| Irritable Bowel Syndrome, Quality of Life (IBS-QOL) | Change from baseline quality of life at 1 month and 3 months |
| Rathus Assertiveness Schedule (RAS) | Change from baseline assertiveness at 1 month and 3 months |
| Emotional Approach Coping Scale (EAC) | Change from baseline emotional approach coping at 1 month and 3 months |
| Communicating Thoughts and Feelings Questionnaire | Change from baseline ability to communicate thoughts and feelings at 1 month and 3 months |
| Clinical Global Impressions (CGI) Improvement Scale - IBS version | Change from baseline IBS symptoms at 1 month and 3 months |
| Health care Utilization Scale | Change in health care utilization from baseline to 1-month and 3-month follow-ups |
| Brief Symptom Inventory | Change in psychological symptoms from baseline to 1-month and 3-month follow-ups |
| Early Trauma Inventory Self-Report Short Form | Change in Trauma reports from baseline to 1-month and 3-month follow-ups |
| Experiences in Close Relationships Questionnaire | Change in attachment from baseline to 1-month and3-month follow-ups |
| General Social Constraints Scale | Change in social constraints from baseline to 1-month and 3-month follow-ups |
| Medication use | Change in medication use from baseline to 1-month and 3-month follow-ups |
| IBS self-efficacy questionnaire | Change from baseline self-efficacy at 1 month and 3 months |
Countries
United States
Outcome results
None listed