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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03064321
Other study ID # K24NR016685-01A1
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date November 1, 2017
Est. completion date March 30, 2020

Study information

Verified date February 2021
Source University of Pittsburgh
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study will test the effect of the an insomnia intervention with cognitive behavioral treatment delivered via web compared with an information control group on glucose control and self management behavioral in a sample of persons with type 2 diabetes (T2DM).


Description:

Recent evidence supports that insomnia is a prevalent problem among persons with type 2 diabetes that may be associated with increased daytime sleepiness and fatigue, increased diabetes-related distress, decreased self-management behavior, and worse glycemic control. The main hypothesis of the current application is that a web-based cognitive behavioral treatment of insomnia (Sleep Health Using the Internet: SHUTi) in persons with T2DM will not only improve their nighttime sleep, but also improve their ability to integrate diabetes education into their daily behavior and positively affect their glucose control compared to a web-based Information Control (IC) group. The aims of this study are to 1) obtain preliminary data to facilitate further hypothesis development and enhance the feasibility of conducting a randomized clinical trial to examine if treatment of insomnia results in participant's being better able to integrate diabetes education into their self-management behavior and result in improved glucose control, 2) explore the associations among changes in insomnia severity, fatigue, daytime sleepiness, sleep quality, A1C (a measure of glucose control over the last three months) and diabetes self-management (DSM) behaviors, 3) explore average pre-intervention to post-intervention changes in insomnia severity, daytime symptoms (fatigue, sleepiness, mood) and DSM behaviors (diet and physical activity) in subjects treated with SHUTi + DSM compared to IC + DSM subjects at 3 months, and 4) explore sleep fragmentation as a potential physiological mechanism linking impaired glucose control (A1C) and sleep in subjects with insomnia and T2DM at baseline and 3 months.


Recruitment information / eligibility

Status Completed
Enrollment 18
Est. completion date March 30, 2020
Est. primary completion date March 30, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - (1) T2DM with suboptimal glucose control - (2) age 18 years or older; - (3) willing to be randomized to SHUTi or IC group; - (4) able to speak, read, and write in English, and - (5) insomnia symptoms with at least one daytime consequence [e.g. impaired mood, poor sleep quality, excessive daytime sleepiness, fatigue]. Exclusion Criteria: - Type 1 or gestational diabetes - Change in oral medications or > 10% change in insulin in last 3 months - Acute medical or psychiatric illness or hospitalization = 3 months (such as angina, stroke, major surgery, major depression or serious psychiatric conditions) - AHI (apnea-hypopnea index; apnea [cessation of breathing] or hypopnea [reduction in breathing]) = 10 episodes an hour on overnight sleep study - Non-ambulatory - Self-reported epilepsy, psychotic or bipolar disorder - History of near-miss or auto accident during last 12 months - Employed in safety sensitive job (e.g. truck driver or airline pilot) - Working nights or rotating shifts - Regular use of alerting (e.g., modafinil) medications - Consumption of alcohol: Men: > 4 drinks a day or > 14 drinks per week - Women: > 3 drinks a day or > 7 drinks per week - If using sleep medications, the drug and/or dose changed in the past month - Depression - Medications for psychotic or bipolar disorders - No internet access - Pregnant or intend to become pregnant in the next four months (postmenopausal or confirmed not pregnant by a urine pregnancy test)

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Insomnia Intervention
The SHUTi intervention is based on a cognitive behavioral treatment for insomnia (CBT-I) and organized into six structured, weekly online sessions. Each week the participants will complete a 30-minute interactive learning module and to complete daily online sleep diaries will be used.
Other:
Information Control
Information on websites that are general health promoting

Locations

Country Name City State
United States University of Pittsburgh School of Nursing Pittsburgh Pennsylvania

Sponsors (1)

Lead Sponsor Collaborator
University of Pittsburgh

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Other Insomnia Severity Scores on the Insomnia Severity Index questionnaire After 12 weeks of either the insomnia intervention or the information control intervention
Primary Average Glucose Control for Last 3 Months Assessed by A!C level A1C level After 12 weeks of either the insomnia intervention or the information control intervention
Secondary Sleep Quality Scores on the Pittsburgh Sleep Quality Index questionnaire After 12 weeks of either the insomnia intervention or the information control intervention
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