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Survivor-Sleep Health Information Program

A Sleep Intervention for Children After Cancer: Survivor Sleep Health Information Program (Survivor-SHIP)

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04863157
Enrollment
16
Registered
2021-04-28
Start date
2021-05-24
Completion date
2022-12-31
Last updated
2023-01-18

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

Conditions

Insomnia, Pediatric Cancer, Sleep Problem

Keywords

Sleep Problem, Insomnia, Pediatric Cancer, Behavioral Intervention

Brief summary

The purpose of the study is to learn if an educational program delivered to parents/guardians can help improve the sleep of children experiencing sleep problems after completing cancer treatment. The name of the intervention is Survivor-SHIP (Sleep Health Information Program).

Detailed description

This study will evaluate Survivor-SHIP in a single-arm trial of 20 off-treatment childhood cancer survivors (ages 5-12). The intervention is an adapted version of the family-centered Sleep Health Program designed at Seattle Children's Hospital. The program offers parents information about how to utilize evidence-based strategies for their child's sleep, and has demonstrated success in a community-based sample of children with behavioral sleep problems. Sessions will focus on providing parents with education about healthy sleep and setting targets for modifiable behaviors that can improve their child's sleep health. The study will include 3 education sessions taking place over videoconference. Families will be asked to track their child's sleep using sleep diaries during the course of the program. Prior to, and following the program, families will be asked to complete study questionnaires.

Interventions

BEHAVIORALSurvivor-SHIP

Parent/guardian education about healthy sleep practices to improve their child's sleep health.

Sponsors

Children's Cancer Research Fund
CollaboratorOTHER
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
5 Years to 12 Years
Healthy volunteers
No

Inclusion criteria

* Child aged 5-12 years, with a history of a cancer diagnosis (except non-melanoma skin cancer). * No cancer therapy (excluding chemoprevention) in the past 6 months, and no further therapy planned. * Child meets diagnostic criteria for insomnia disorder as determined by insomnia screening criteria (see Appendix A) * Parent/guardian is able to read and write in English. * Regular access to a computer/smartphone with internet access at home.

Exclusion criteria

* Reports child has been diagnosed with a Seizure Disorder or has experienced a seizure in the past 12 months. * Reports child has been diagnosed with a developmental disorder such as Autism Spectrum Disorder, Cerebral Palsy, Fragile X Syndrome, or Moderate to Profound Intellectual Disability. * Reports child has been diagnosed with sleep apnea, and are not receiving recommended medical treatment for their sleep apnea. * Intention to adjust (decrease or increase) child's use of any prescribed or over-the-counter sleep medications during the study period. * Any impairment (e.g., hearing, visual, cognitive) that interferes with the parent/guardian's ability to complete all study procedures independently.

Design outcomes

Primary

MeasureTime frameDescription
Intervention acceptability6 weeksIntervention acceptability will be assessed using the Satisfaction subscale of the Usability, Satisfaction, and Ease of use (USE) scale. Total scores will range from 0-11, with higher scores indicating better acceptability.
Intervention feasibility6 weeksIntervention feasibility will be assessed based on adherence rates to the intervention sessions.

Secondary

MeasureTime frameDescription
Sleep quality6 weeksThe Patient-reported outcomes measurement information system (PROMIS) pediatric sleep scales are an 8-item measure that assesses the child's sleep quality. A total score will range from 8 to 40, with higher scale scores indicating poorer sleep health
General quality of life6 weeksThe child's quality of life will be evaluated by the Pediatric Quality of Life Inventory (PedsQL), a 23-item scale measuring core physical, mental, and social health dimensions. Scores are transformed on a scale from 0 to 100, with higher scores indicating better function.
Sleep knowledge6 weeksThe Parent Sleep Knowledge questionnaire is a 10-item questionnaire assessing the parents' knowledge about children's sleep. The scale is scored from 0 to 10, with a higher score indicating more knowledge.
Sleep change6 weeksThe investigators will assess whether the family implemented any non-intervention advised changes to their child's sleep routine, such as increasing medication for their sleep during the intervention period. This set of 5 questions will be assessed only at the post-intervention timepoint.
Screen time6 weeksThe extent of the child's electronic screen use will be assessed by a set of 9 questions that were developed specifically for this study by the Principal Investigator. They assess the duration of electronics usage across different devices and timing of usage.
Sleep habits6 weeksThe Children's Sleep Habits Questionnaire (CSHQ) is a 33-item questionnaire that will assess the child's overall sleep habits. A Total Sleep Disturbances score is calculated as the sum of all scored questions, and can range from 33 to 99, with higher scores indicating more sleep disturbance.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026