Clinical trial · Interventional
Developing and Pre-Testing an eHealth Group Intervention for Young Adult Cancer Survivors
NCT05054569CI-TRIAL-00055784completedN/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 this study is to develop and pre-test an eHealth group intervention for young adult cancer survivors.
Conditions
Conditions (1)
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 | Malignant Neoplasm | ALIAS | 0.90 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Cognitive-Behavioral Stress Management and Health Education | Behavioral | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- 10-week eHealth intervention
- description
- Weekly video conference groups led by a trained facilitator
- interventionNames
- Behavioral: Cognitive-Behavioral Stress Management and Health Education
Primary outcomes (3)
- measure
- Acceptability of the adapted intervention
- timeFrame
- Over the course of the 10-week intervention, beginning with the first weekly session through the tenth weekly session
- description
- Participants will report their satisfaction with individual sessions through brief weekly surveys.
- measure
- Acceptability of the adapted intervention
- timeFrame
- Over the course of the 10-week intervention, beginning with the first weekly session through the tenth weekly session
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 39 Years
Show eligibility criteria text
Inclusion Criteria: * age 18-39 years at the time of participation * diagnosed with a non-metastatic primary cancer between 18-39 years old * completed primary cancer treatment (excepting hormone therapy) 1 month to 5 years prior to enrollment * able to speak and read English * access to internet or cellular connectivity with sufficient bandwidth to participate in videoconferences Exclusion Criteria: * metastatic disease * psychiatric or neurological disorders that could interfere with study participation * considered part of a vulnerable population
References
Publications (2)
- DERIVEDFox RS, Badger TA, Moya S, Gudenkauf LM, Nelson MA, O'Neill RM, Leete JJ, Friedman SE, Katsanis E, Victorson DE, Sanford SD, Penedo FJ, Antoni MH, Oswald LB. An HRQOL Proof-Of-Concept Analysis of the eHealth TOGETHER Intervention for Adolescent and Young Adult Cancer Survivors: A Brief Report. Psychooncology. 2025 Jul;34(7):e70234. doi: 10.1002/pon.70234. PMID 40879639
- DERIVEDOswald LB, Lyleroehr M, Gudenkauf LM, Armstrong GE, Tometich DB, Sanford SD, Loecher N, Geiss C, Rodriguez Y, Scheel KL, Nieves-Lopez A, Jim HSL, Gonzalez BD, Antoni MH, Penedo FJ, Reed D, Katsanis E, Salsman JM, Victorson D, Fox RS. Development and initial testing of TOGETHER-YA: an eHealth-delivered and group-based psychosocial intervention for young adult cancer survivors. Support Care Cancer. 2022 Dec;30(12):10067-10076. doi: 10.1007/s00520-022-07382-y. Epub 2022 Oct 14. PMID 36229547