Clinical trial · Interventional
Innovating CBT-I for Cancer Survivors: An Optimization Trial
- 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 overall goal of this project is to conduct a factorial, randomized controlled trial to optimize synchronous, virtual delivery of CBT-I for cancer survivors. The proposed project will yield multiple deliverables to innovate cancer survivorship care, chiefly an optimized, scalable, virtually-delivered intervention that addresses chronic insomnia, one of the most deleterious concerns among the growing demographic of cancer survivors in the U.S. Findings will inform future considerations for delivering CBT-I to cancer survivors.
Conditions
Conditions (2)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Cancer Survivorship | — | UNRESOLVED | — |
| Insomnia | — | UNRESOLVED | — |
Interventions
Interventions (4)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Survivorship Sleep Program with Group Delivery + 3 Booster Sessions | Behavioral | — | UNRESOLVED |
| Survivorship Sleep Program with Group Delivery + No Booster Sessions | Behavioral | — | UNRESOLVED |
| Survivorship Sleep Program with Individual Delivery + 3 Booster Sessions | Behavioral | — | UNRESOLVED |
| Survivorship Sleep Program with Individual Delivery + No Booster Sessions | Behavioral | — | UNRESOLVED |
Design
Arms and outcomes
Arms (4)
- type
- EXPERIMENTAL
- label
- Group 1: Survivorship Sleep Program with Individual Delivery + No Booster Sessions
- description
- 4 weekly SSP sessions delivered to individual participants (session durations approximately 45 min/session). No booster sessions.
- interventionNames
- Behavioral: Survivorship Sleep Program with Individual Delivery + No Booster Sessions
- type
- EXPERIMENTAL
- label
- Group 2: Survivorship Sleep Program with Group Delivery + No Booster Sessions
- description
- 4 weekly SSP sessions delivered to groups of participants (session durations approximately 90 min/session). No booster sessions.
- interventionNames
- Behavioral: Survivorship Sleep Program with Group Delivery + No Booster Sessions
- type
- EXPERIMENTAL
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * History of nonmetastatic, localized, or regional solid or blood malignancy(ies) * Completion of primary cancer treatment (radiation, surgery, and/or chemotherapy). Use of hormonal, maintenance, oral, and immunotherapies is permitted. * Chronic insomnia (DSM-5 criteria) * 18 years of age or older Exclusion Criteria: * Self-reported inability to speak and write in English * Undertreated noninsomnia sleep disorder (e.g., sleep apnea) * Undertreated epilepsy, undertreated serious mental illness, undertreated suicidality, and/or psychiatric hospitalization in the past year * Unwilling or unable to discontinue night shift work
References
Publications (0)
Data not yet available