Clinical trial · Interventional
iCanWork: A Randomized Controlled Trial
Effects of the iCanWork Intervention to Improve Cancer Survivors' Experience With Return to Work: A Randomized Controlled Trial (RCT)
NCT05546736CI-TRIAL-00061036iCanWorkunknownN/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 aim of this study is to evaluate the effectiveness of the iCanWork intervention in assisting cancer survivors (CS) to return to work (RTW) and its impact on their health-related quality of life (QoL), health service utilization, RTW readiness, time to RTW, and work capacity.
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 |
|---|---|---|---|
| Cancer-related Problem/Condition | — | UNRESOLVED | — |
| Quality of Life | — | UNRESOLVED | — |
| Survivorship | — | UNRESOLVED | — |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| iCanWork Intervention | Behavioral | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- iCanWork Intervention
- description
- iCanWork includes 6 1-hour sessions with a VRC and 1 to 4 1-hour sessions with an OT. In the positive event that a participant has returned to work during the study, three of the six VRC sessions are reserved to support the participants in their transition to the workplace.
- interventionNames
- Behavioral: iCanWork Intervention
- type
- NO_INTERVENTION
- label
- Control
- description
- Participants randomized to the control group will receive their usual care and will be referred to the Cancer Work website for educational resources related to RTW. If they contact the team with RTW-related questions, they will be referred to their care teams.
Primary outcomes (1)
- measure
- Change from baseline return to work status in the course of the 24-month study
- timeFrame
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 65 Years
Show eligibility criteria text
Inclusion Criteria: * diagnosed with cancer (all types) treated with curative intent and of working age (between 18 and 65 at the time of diagnosis) * gainfully employed at the time of diagnosis (full or part-time, including students) * still on sick leave, including long-term disability leave, but for less than 2 years * has not started to return to work, since stopping due to cancer * can read and understand English or French * reside in Canada. Exclusion Criteria: \- If the cancer survivor's physicians consider returning to work unwise, such as due to a metastatic cancer diagnosis
References
Publications (0)
Data not yet available
No reference posted for this study.