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Treating Disrupted Sleep in Individuals With Inflammatory Bowel Disease

Primary Purpose

Sleep Disturbance, Fatigue, Inflammatory Bowel Disease

Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Behavioral Counseling
bupropion-SR
Sponsored by
Eva Szigethy
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Sleep Disturbance focused on measuring Inflammatory Bowel Disease, Physical Illness, Wellbutrin

Eligibility Criteria

15 Years - 30 Years (Child, Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • IBD Group:

    • Biopsy confirmed Crohn's Disease
    • Qualifying scores on Multidimensional Fatigue Inventory and Pittsburgh Sleep Quality Index
  • Healthy Volunteer Group:

    • Does not meet any exclusion criteria

Exclusion Criteria:

  • IBD Group:

    • Meeting criteria for active alcohol or substance abuse or dependence
    • Current ongoing treatment with Wellbutrin
    • Females who are pregnant or plan to become pregnant within three months
    • Sleep disorder such as apnea, restless leg syndrome or use of Continuous positive airway pressure therapy (C-PAP)/Bilevel positive airway pressure (Bi-PAP)
    • Current IBD flare requiring hospitalization with intravenous steroid treatment
    • Other acute medical conditions or a history of chronic inflammatory condition other than IBD
    • Hemoglobin <10 with age and gender adjustments
    • History of seizure disorder
    • Acute infection within seven days
  • Healthy Volunteer Group:

    • History or current episode of psychiatric disorder by Diagnositic and Statistical Manual (DSM-IV)
    • Current ongoing treatment with psychoactive medications
    • Medications for sleep in previous two weeks
    • Females who are pregnant or plan to become pregnant within three months
    • History of IBD, epilepsy, rheumatoid arthritis, lupus
    • Sleep disorder such as apnea, restless leg syndrome or use of Continuous positive airway pressure therapy (C-PAP)/Bilevel positive airway pressure (Bi-PAP)

Sites / Locations

  • Presbyterian University Hospital of UPMC
  • Children's Hospital of Pittsburgh

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Other

Other

No Intervention

Arm Label

Behavioral Counseling

Behavioral counseling + bupropion-SR

Healthy Control

Arm Description

Brief Behavioral Therapy for Sleep Disruption in IBD (BBTS-I). This treatment phase focuses on treating insomnia, a nighttime component of sleep disturbance delivered in 1:1 sessions which can be completed in person or by phone, except for initial session.

Brief Behavioral Therapy for Sleep Disruption in IBD (BBTS-I) plus bupropion-SR (bupropion-Sustained Release). 8-week trial of bupropion-SR (target dose: 200-300 mg/day). bup-SR, a noradrenergic dopaminergic reuptake inhibitor (NDRI). NDRI has been shown to improve fatigue and rapid eye movement-sleep (REM) in medically ill populations.

The healthy control group includes individuals who are free of physical and psychiatric illness between the ages of 15-30.

Outcomes

Primary Outcome Measures

Change From Baseline in Multidimensional Fatigue Inventory (MFI) for Each Arm
MFI score range is 0-100. Higher score indicates higher level of fatigue.
Change in Baseline in Pittsburgh Sleep Quality Index (PSQI) for Each Arm
PSQI score range is 0-21 with higher score indicating greater sleep disturbance.

Secondary Outcome Measures

Full Information

First Posted
June 11, 2014
Last Updated
August 14, 2017
Sponsor
Eva Szigethy
Collaborators
Crohn's and Colitis Foundation
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1. Study Identification

Unique Protocol Identification Number
NCT02162862
Brief Title
Treating Disrupted Sleep in Individuals With Inflammatory Bowel Disease
Official Title
Treating Disrupted Sleep in Individuals With Inflammatory Bowel Disease: A Novel Adjunctive Therapy for Chronic Inflammatory Illness
Study Type
Interventional

2. Study Status

Record Verification Date
June 2017
Overall Recruitment Status
Completed
Study Start Date
July 2013 (Actual)
Primary Completion Date
June 30, 2016 (Actual)
Study Completion Date
June 30, 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Eva Szigethy
Collaborators
Crohn's and Colitis Foundation

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to determine if either a targeted type of talk therapy (Phase I) or medication, Wellbutrin, (Phase II) improve sleep disturbance and/or fatigue in individuals with Inflammatory Bowel Disease (IBD).
Detailed Description
The present study, sponsored by the Crohn's and Colitis Foundation of America, intends to provide information about the feasibility and effectiveness of treatments designed to lessen fatigue and improve sleep among youth with Crohn's disease (CD). Obtaining good sleep is vital in leading a healthy life. For youth with Inflammatory Bowel Disease (IBD), good sleep is key as patients are psychically and psychologically developing and maturing. Previous work suggests that 42% of youth with CD experience poor sleep: difficulty falling asleep, disruption in sleep, early morning awakening, or an absence of feeling refreshed after sleep. Poor sleep can negatively affect ones physical health, mental health, and stress level - each minimizing ones quality of life. Participants in the study range from 15-30 years old, live with CD, and experience sleep disturbances, targeting 100 participants. Additionally, a healthy control group, 30 participants, is included for comparison. The study contains two phases and takes place over a 12-week period. Phase one involves partaking in 3-8 sessions of Brief Behavioral Therapy for Sleep in IBD (BBTS-I) with study clinician. The treatment teaches self-management techniques and sleep interventions through self-hypnosis/relaxation and reflection. After the treatment, participants are reevaluated. Those who respond well to the treatment are offered 1-2 booster sessions, those who do not show improvement move on to phase two. In phase two, participants are offered an 8-week course of bupropion-sustained release (BUP-SR). BUP-SR reduces fatigue, depression, and inflammation, and enhances REM sleep. The prescribed dosage will increase from 100mg to 300 mg (150 mg 2x a day). Participant's characterization measures are assessed at the start, midpoint, and finish of the study to measure changes in sleep, fatigue, and mood. Also at these times, blood work is done in hopes of gaining an understanding of the cause of CD. At each of the three assessments, participants are asked to wear a wristwatch device for 7 days that records: total sleep time, wakefulness, and daytime information on napping and sleep hygiene. In addition, participants are asked to keep a brief sleep diary for a 7-day period. This study hopes to provide new treatments to increase the quality of life, primarily by improving sleep in patients with CD.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Sleep Disturbance, Fatigue, Inflammatory Bowel Disease
Keywords
Inflammatory Bowel Disease, Physical Illness, Wellbutrin

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Factorial Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
99 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Behavioral Counseling
Arm Type
Other
Arm Description
Brief Behavioral Therapy for Sleep Disruption in IBD (BBTS-I). This treatment phase focuses on treating insomnia, a nighttime component of sleep disturbance delivered in 1:1 sessions which can be completed in person or by phone, except for initial session.
Arm Title
Behavioral counseling + bupropion-SR
Arm Type
Other
Arm Description
Brief Behavioral Therapy for Sleep Disruption in IBD (BBTS-I) plus bupropion-SR (bupropion-Sustained Release). 8-week trial of bupropion-SR (target dose: 200-300 mg/day). bup-SR, a noradrenergic dopaminergic reuptake inhibitor (NDRI). NDRI has been shown to improve fatigue and rapid eye movement-sleep (REM) in medically ill populations.
Arm Title
Healthy Control
Arm Type
No Intervention
Arm Description
The healthy control group includes individuals who are free of physical and psychiatric illness between the ages of 15-30.
Intervention Type
Behavioral
Intervention Name(s)
Behavioral Counseling
Intervention Type
Drug
Intervention Name(s)
bupropion-SR
Other Intervention Name(s)
Wellbutrin
Primary Outcome Measure Information:
Title
Change From Baseline in Multidimensional Fatigue Inventory (MFI) for Each Arm
Description
MFI score range is 0-100. Higher score indicates higher level of fatigue.
Time Frame
Baseline (week 0) to end of study (week 14)
Title
Change in Baseline in Pittsburgh Sleep Quality Index (PSQI) for Each Arm
Description
PSQI score range is 0-21 with higher score indicating greater sleep disturbance.
Time Frame
Baseline (week 0) to end of study (week 14)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
15 Years
Maximum Age & Unit of Time
30 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: IBD Group: Biopsy confirmed Crohn's Disease Qualifying scores on Multidimensional Fatigue Inventory and Pittsburgh Sleep Quality Index Healthy Volunteer Group: Does not meet any exclusion criteria Exclusion Criteria: IBD Group: Meeting criteria for active alcohol or substance abuse or dependence Current ongoing treatment with Wellbutrin Females who are pregnant or plan to become pregnant within three months Sleep disorder such as apnea, restless leg syndrome or use of Continuous positive airway pressure therapy (C-PAP)/Bilevel positive airway pressure (Bi-PAP) Current IBD flare requiring hospitalization with intravenous steroid treatment Other acute medical conditions or a history of chronic inflammatory condition other than IBD Hemoglobin <10 with age and gender adjustments History of seizure disorder Acute infection within seven days Healthy Volunteer Group: History or current episode of psychiatric disorder by Diagnositic and Statistical Manual (DSM-IV) Current ongoing treatment with psychoactive medications Medications for sleep in previous two weeks Females who are pregnant or plan to become pregnant within three months History of IBD, epilepsy, rheumatoid arthritis, lupus Sleep disorder such as apnea, restless leg syndrome or use of Continuous positive airway pressure therapy (C-PAP)/Bilevel positive airway pressure (Bi-PAP)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Eva Szigethy, MD, PhD
Organizational Affiliation
University of Pittsburgh
Official's Role
Principal Investigator
Facility Information:
Facility Name
Presbyterian University Hospital of UPMC
City
Pittsburgh
State/Province
Pennsylvania
ZIP/Postal Code
15213
Country
United States
Facility Name
Children's Hospital of Pittsburgh
City
Pittsburgh
State/Province
Pennsylvania
ZIP/Postal Code
15224
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

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Treating Disrupted Sleep in Individuals With Inflammatory Bowel Disease

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