Clinical trial · Observational
Patient Communication Training Intervention
A Feasibility Study of a Patient Communication Training Intervention
NCT00933855CI-TRIAL-00005811completedClinicalTrials.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 test a class for Queens Cancer Center patients. We want to find out if patients think this program is helpful.
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 |
|---|---|---|---|
| Questionnaires and training workshop | Behavioral | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- label
- communication training workshop
- description
- The patient intervention is a 1 hour communication workshop entitled: "Getting the Most out of your Doctor's Visit." The workshops will be offered to both patients and family members, but data will be collected only for patients. The workshops will be held on location at Queens Cancer Center.
- interventionNames
- Behavioral: Questionnaires and training workshop
Primary outcomes (1)
- measure
- To determine the feasibility of a patient communication training intervention.
- timeFrame
- 2 years
Secondary outcomes (2)
- measure
- To attain preliminary data on the acceptability of the intervention through patient ratings of effectiveness and usefulness of the intervention.
- timeFrame
- 2 years
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * Patients seeing a physician at Queens Cancer Center (not family members or partners) * Able to provide informed consent. Exclusion Criteria: * Less than 18 years of age (as per self-report) * Cognitive or physical impairment rendering patients incapable of providing informed consent to participate in the study. * As the workshop will be given in English and the measures are all written in English, subjects who are not fluent in English will be excluded.
References
Publications (0)
Data not yet available
No reference posted for this study.