ClinicalTrials.Veeva

Menu

Self-Management in Young Adults With Type 1 Diabetes (SLEEPT1D)

Case Western Reserve University logo

Case Western Reserve University

Status

Completed

Conditions

Type 1 Diabetes

Treatments

Behavioral: Sleep Self-Management

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT04975230
R00NR018886 (U.S. NIH Grant/Contract)
STUDY20201829
K99NR018886 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

Type 1 Diabetes (T1D) affects 1.6 million Americans, and only 14% of young adults age 18-25 years achieve glycemic targets (glycosylated hemoglobin A1C <7.0%). Achieving glycemic targets is associated with reduced risk for both micro-and macrovascular complications, better neurocognitive function, and better diabetes quality of life. In lab studies, sleep deprivation led to impaired glucose tolerance and insulin sensitivity in adults without chronic condition and in one study of adults with T1D. Extending sleep in natural environments contributes to improved insulin sensitivity and glucose levels, neurocognition, and psychological symptoms in young adults without chronic conditions. Modifiable dimensions of sleep health (appropriate sleep duration, stability, and timing) are associated with better glycemic control in adults with T1D. Therefore, improving sleep duration, stability, and timing may be potential therapeutic targets to improve glucoregulation and clinical outcomes (diabetes self-management, neurocognitive function, and symptoms) in this high-risk population.

The overall objective is to test and compare the effects of a cognitive-behavioral sleep self-management intervention (sleep extension and consistency in sleep timing) compared to an attention control condition (habitual sleep duration + diabetes self-management education) on improving sleep duration, stability, and timing, and glycemia (glycemic control and glucose variability) in short-sleeping young adults with T1D in a pilot randomized controlled trial.

Full description

This is a two-arm randomized controlled trial, with participants assigned to either the Sleep Self-Management arm or the attention control arm (Diabetes Self-Management Education). The Sleep Self-Management condition involves an initial 50-minute face-to-face consultation with brief 5-10 minute weekly follow-ups in a format TBD by aim 1 (e.g., call, text, video conference) with 3-week booster sessions in person. The Sleep Self-Management intervention activities are provided in addition to "usual care."

Enrollment

39 patients

Sex

All

Ages

18 to 26 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 1) Age range: from 18 to 26 years
  • 2) Diagnosed with T1D for at least 6 months
  • 3) No other major health problems (e.g., chronic medical condition or major psychiatric illness
  • 4) Not currently participating in any intervention studies
  • 5) Read/speak English
  • 6) Have a most recent A1C or eA1C value ≥ 7%.

Exclusion criteria

  • 1) Previous OSA diagnosis/high-risk sleep apnea
  • 2) Current pregnancy
  • 3) Night shift workers
  • 4) Habitually sleep > 7 hours on work or school days.

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

39 participants in 2 patient groups

Sleep Self-Management
Experimental group
Description:
The Sleep Self-Management Intervention involves an initial 50-minute face-to-face interactive session in a private location. Participants are asked to extend time in bed by 1 hour and consistently maintain the extension on both weekends and weekdays. Bedtimes and waketimes will be assessed to ascertain which time is most modifiable for the participant's lifestyle and routine. There will be weekly follow-ups and in-person 3-week booster sessions. Sleep reports generated by the actigraphy will be shared with participants with brief action planning and goal setting to address progress towards goal achievement. A need to revise plans for future weeks will be the booster sessions' major goal.
Treatment:
Behavioral: Sleep Self-Management
Diabetes Self-Management Education
No Intervention group
Description:
The Attention Control arm will receive Diabetes Self-Management Education at the initial consultation visit via in-person contact at T1. There will be weekly follow-ups and in-person 3-week sessions. A Diabetes Self-Management Tracking Form will be used to monitor the weekly acquisition of information and plans for the 6-week intervention and at the 3-month and 6-month data points.

Trial documents
3

Trial contacts and locations

1

Loading...

Central trial contact

Mary Leuchtag, MSSA; Stephanie Griggs, PhD

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems