Clinical trial · Interventional
Survivorship Care Planning in Patients With Colorectal or Non-Small Cell Lung Cancer
Survivorship Care Planning in Colorectal and Lung Cancer: A Feasibility Study
NCT01741636CI-TRIAL-00013072completedN/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)
Survivorship Care Planning may improve overall well-being and quality of life of colorectal and lung cancer survivors
Conditions
Conditions (20)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Stage IA Non-small Cell Lung Cancer | Lung Non-Small Cell Carcinoma | CURATED_BROADER | 0.78 |
| Stage IB Non-small Cell Lung Cancer | Lung Non-Small Cell Carcinoma | CURATED_BROADER | 0.78 |
| Stage I Colon Cancer | Malignant Colon Neoplasm | CURATED_BROADER | 0.78 |
| Stage IIA Colon Cancer | Malignant Colon Neoplasm | CURATED_BROADER | 0.78 |
| Stage IIA Non-small Cell Lung Cancer | Lung Non-Small Cell Carcinoma | CURATED_BROADER | 0.78 |
| Stage IIA Rectal Cancer | Malignant Rectal Neoplasm | CURATED_BROADER | 0.78 |
| Stage IIB Colon Cancer | Malignant Colon Neoplasm | CURATED_BROADER | 0.78 |
| Stage IIB Non-small Cell Lung Cancer | Lung Non-Small Cell Carcinoma | CURATED_BROADER | 0.78 |
Interventions
Interventions (3)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| educational intervention | Other | — | UNRESOLVED |
| quality-of-life assessment | Procedure | — | UNRESOLVED |
| questionnaire administration | Other | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- Supportive care (survivorship plan)
- description
- Patients undergo Survivorship Care Planning comprising disease surveillance, management of potential long-term and late effects, psycho-social-spiritual issues, and healthy living recommendations.
- interventionNames
- Other: educational intervention
- Other: questionnaire administration
- Procedure: quality-of-life assessment
Primary outcomes (6)
- measure
- Percentage of attrition based on number of patients who failed to complete the two-month study
- timeFrame
- 2 months
- description
- Descriptive statistics will be presented on those who agree to participate and the proportion of those approached who agree to participate.
- measure
- Total retention across the two month follow-up
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 21 Years
Show eligibility criteria text
Inclusion Criteria: * Pathologically confirmed diagnosis of stage I, II, or III CRC or NSCLC * Able to read and understand English * Able to read and/or understand the study protocol requirements, and provide written informed consent * Diagnosis of CRC or NSCLC * Within three months of completing primary treatment (surgery, chemotherapy, radiation, or chemoradiation) * Without recurrent or new primary cancers
References
Publications (0)
Data not yet available
No reference posted for this study.