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Web-based Insomnia Treatment for Adolescent and Young Adult Cancer Survivors

Web-based Insomnia Treatment for Adolescent and Young Adult Cancer Survivors

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03279055
Enrollment
22
Registered
2017-09-12
Start date
2018-08-10
Completion date
2019-12-20
Last updated
2020-10-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Insomnia

Keywords

Insomnia

Brief summary

This research study is evaluating a six-session online program designed to help insomnia (difficulty falling or staying asleep) in adolescent and young adult cancer survivors.

Detailed description

The purpose of this study is to learn whether an adapted version of SHUTi (Sleep Healthy Using the Internet), a six-session online program which has been found to be effective in other groups of people, will be useful in treating insomnia in adolescent and young adult cancer survivors.

Interventions

BEHAVIORALSHUTi

Sleep Healthy Using the Internet (SHUTi) is a publicly available insomnia intervention program. It focuses on 5 treatment components that form the core of CBT-I: sleep restriction, stimulus control, cognitive restructuring, sleep behaviors, and relapse prevention.

Sponsors

Alex's Lemonade Stand Foundation
CollaboratorINDUSTRY
Dana-Farber Cancer Institute
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
14 Years to 25 Years
Healthy volunteers
No

Inclusion criteria

* 14-25 years of age * History of a cancer diagnosis * No active cancer therapy (excluding chemoprevention) in the past three months, and no cancer therapy currently planned in the next 6 months * No surgery planned in the next 6 months * Significant insomnia as evidenced by an Insomnia Severity Index score ≥12 * Able to read and write in English * Has internet access at home * Motivated and able to follow the demands of the SHUTi program, to keep sleep records, complete self-report symptom reports and make changes in their sleep schedule, including restricting their sleep

Exclusion criteria

* Prior attempt(s) to treat insomnia using cognitive-behavioral treatment for insomnia * History of Bipolar Disorder diagnosis * History of a Seizure Disorder diagnosis or have experienced a seizure in the past 12 months * Intention to adjust (decrease or increase) use of sedative, hypnotic, or over-the-counter (e.g., Benadryl, Unisom) medications that can affect sleep during the study period * Diagnosed, untreated sleep apnea or sleep apnea suspected by a physician but which has not been unevaluated, or other sleep disorder * Employment that involves irregular sleep patterns, such as shift-work or frequent long-distance travel that involves adjusting to different time zones, or employment in a position that could impact public safety (such as operating heavy machinery) * Refusal to modify or reduce excessive alcohol use that is likely to interfere with an individual's sleep

Design outcomes

Primary

MeasureTime frameDescription
Insomnia symptoms8 weeksInsomnia symptom severity will be assessed using the Insomnia Severity Index

Secondary

MeasureTime frameDescription
Sleep efficiency6 weeksSleep diary calculated sleep efficiency
Quality of life8 weeksMeasured with PedsQL
Daytime sleepiness8 weeksMeasured with Pediatric Daytime Sleepiness Scale

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 18, 2026