Assessing Medical Trial Experiences of Hairy Cell Leukemia Patients
Not yet recruiting
- Conditions
- Hairy Cell Leukemia
- Registration Number
- NCT05859932
- Lead Sponsor
- Power Life Sciences Inc.
- Brief Summary
The percentages of participants in clinical studies haven't always been perfectly representative of a particular group.
This research examines the variables that affect a patient's choice to enroll in, discontinue participation in, or resume participation in a clinical trial for hairy cell leukemia.
It will also try to analyze data from the perspective of different demographic groups to check for recurring trends which might yield insights for the sake of hairy cell leukemia studies.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- NOT_YET_RECRUITING
- Sex
- All
- Target Recruitment
- 500
Inclusion Criteria
- Aged ≥ 18 years old
- Ability to understand and the willingness to sign a written informed consent document.
- Willing and able to comply with scheduled visits, treatment schedule, laboratory tests and other requirements of the study.
Exclusion Criteria
- Is pregnant, breastfeeding or expecting to conceive within the projected duration of the study
- Any mental or medical condition that prevents the patient from giving informed consent or participating in the trial
- Patients with any significant history of non-compliance to medical regimens or with inability to grant a reliable informed consent.
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Rate of patients who decide to enroll in a hairy cell leukemia clinical study. 3 months Number of hairy cell leukemia study participants who remain in clinical trial until completion. 12 months
- Secondary Outcome Measures
Name Time Method