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Development of a Scale for Cancer Patients' Willingness to Voluntarily Participate in Drug Clinical Trials

Sun Yat-sen University logo

Sun Yat-sen University

Status

Enrolling

Conditions

Cancer

Study type

Observational

Funder types

Other

Identifiers

NCT06120335
SYSKY-2023-1029-01

Details and patient eligibility

About

The goal of this observational study is to develop a scale for cancer patients' willingness to voluntarily participate in drug clinical trials and evaluate its reliability and validity.

Full description

Inclusion Criteria:

  1. Age 18-80 years old (including boundary values).
  2. Tumor patients with clear diagnosis.
  3. Whether they finally sign the informed consent form of one drug clinical trial or not, and whether they are finally enrolled in one drug clinical trial or not, patients who have undergone the informed consent process of drug clinical trials conducted by clinicians can be enrolled in this study.
  4. Volunteer to participate in this study and sign an informed consent form.

Exclusion Criteria:

  1. Patients with unclear consciousness.
  2. Patients who are unable to correctly understand and answer questions.
  3. Vulnerable subjects include: students and subordinates of researchers, military personnel, prisoners, patients with incurable diseases, patients in critical situations, those admitted to welfare institutions, homeless individuals, minors, and those who are unable to provide informed consent.

Enrollment

20 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Age 18-80 years old (including boundary values).
  2. Tumor patients with clear diagnosis.
  3. Whether they finally sign the informed consent form of one drug clinical trial or not, and whether they are finally enrolled in one drug clinical trial or not, patients who have undergone the informed consent process of drug clinical trials conducted by clinicians can be enrolled in this study.
  4. Volunteer to participate in this study and sign an informed consent form.

Exclusion criteria

  1. Patients with unclear consciousness.
  2. Patients who are unable to correctly understand and answer questions.
  3. Vulnerable subjects include: students and subordinates of researchers, military personnel, prisoners, patients with incurable diseases, patients in critical situations, those admitted to welfare institutions, homeless individuals, minors, and those who are unable to provide informed consent.

Trial contacts and locations

1

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Central trial contact

Caie Chen

Data sourced from clinicaltrials.gov

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