Clinical trial · Observational
Development of a Clinical Trial Specific Question Prompt List
- 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 a Question Prompt List (QPL) about clinical trials for cancer patients and find out what cancer patients and their caregivers think of the QPL. A QPL is a list of questions patients might want to ask their doctors during their appointments. We will conduct three focus groups to talk about using QPL's as a new way to recruit patients like you to clinical trials. The three groups will be made of patients who have and have not participated in clinical trials, their caregivers and doctors. This study is also being done to learn about how the QPL affects the question asking behavior of patients during their appointments with doctors at Memorial SloanKettering Cancer Center (MSKCC).
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 |
|---|---|---|---|
| Breast Cancer | Malignant Breast Neoplasm | CURATED_EXACT | 0.92 |
| Lung Cancer | Malignant Lung Neoplasm | CURATED_EXACT | 0.92 |
| Prostate Cancer | Malignant Prostate Neoplasm | CURATED_EXACT | 0.92 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| focus groups | Behavioral | — | UNRESOLVED |
Design
Arms and outcomes
Arms (3)
- label
- 1
- description
- Trial experienced cancer patients and their primary caregivers.
- interventionNames
- Behavioral: focus groups
- label
- 2
- description
- Trial naive cancer patients and their caregivers.
- interventionNames
- Behavioral: focus groups
- label
- 3
- description
- Health care professionals who are involved in running Phase I, II or III clinical trials.
- interventionNames
- Behavioral: focus groups
Primary outcomes (1)
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * Population Segment 1 who have participated in a clinical trial * Diagnosis and treatment at MSKCC of lung, prostate or breast cancer * Completion of a Phase I, II, or III clinical trial at MSKCC * Ability to provide informed consent Patient caregiver eligibility requirements will be: * Nomination by patient as the primary caregiver * Ability to provide informed consent Population Segment 2 who have not participated in a clinical trial: * Diagnosis and treatment at MSKCC of lung, prostate or breast cancer or the primary patient caregiver * Ability to provide informed consent Patient caregiver eligibility requirements will be: * Nomination by patient as the primary caregiver * Ability to provide informed consent Population Segment 3 who are health care professionals: * A current health care professional at MSKCC * Current involvement in recruiting patients with lung, prostate or breast cancer to Phase I,II, or III clinical trials at MSKCC * Ability to provide informed consent Exclusion Criteria: Potential subjects will be considered ineligible for either/both phases of this study if they are: * Fewer than 18 years of age * Cognitively or physically impaired, rendering them incapable of providing informed consent to participate in the study * Population Segment 2 participants will be excluded if they have ever participated in a clinical trial.
References
Publications (0)
Data not yet available