Clinical trial · Interventional
Survivor-Sleep Health Information Program
A Sleep Intervention for Children After Cancer: Survivor Sleep Health Information Program (Survivor-SHIP)
NCT04863157CI-TRIAL-00063267completedN/AClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
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).
Conditions
Conditions (3)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Insomnia | — | UNRESOLVED | — |
| Pediatric Cancer | Childhood Malignant Neoplasm | ALIAS | 0.90 |
| Sleep Problem | — | UNRESOLVED | — |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Survivor-SHIP | Behavioral | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- Survivor-SHIP
- description
- Parents/guardians will take part in 3 education sessions over a one month period. During the sessions, they will learn more about common sleep problems following cancer treatment and ways to understand their child's unique patterns. They will then be educated about behavioral changes they can make to improve their child's sleep.
- interventionNames
- Behavioral: Survivor-SHIP
Primary outcomes (2)
- measure
- Intervention acceptability
- timeFrame
- 6 weeks
- description
- Intervention 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.
- measure
- Intervention feasibility
- timeFrame
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 5 Years
- Maximum age
- 12 Years
Show eligibility criteria text
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.
References
Publications (0)
Data not yet available
No reference posted for this study.