Rectal Cancer
Conditions
Keywords
Rectal Cancer
Brief summary
The primary objective of this research study is to explore the barriers encountered by specific demographic groups of rectal cancer patients during the engagement in clinical trials, which historically lack diverse representation. By carefully analyzing data from various demographic perspectives, this study aims to uncover patterns that impact the experiences of future rectal cancer patients. Active involvement in this crucial research is of utmost importance, as it can offer unique insights to enhance the participation and completion rates of rectal cancer patients in clinical study.
Interventions
None listed
Sponsors
Power Life Sciences Inc.
Study design
Observational model
CASE_CROSSOVER
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Confirmed diagnosis of rectal cancer * Aged ≥ 18 years old and ability to provide written informed consent obtained prior to participation in the study and any related procedures being performed * No prior treatment for rectal cancer
Exclusion criteria
* Pregnant or lactating woman * Inability to provide written informed consent * Enrolled in another research study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Number of rectal cancer patients who decide to participate in a clinical study | 3 months |
| Rate of patients who remain in a rectal cancer clinical study to completion | 12 months |
Countries
United States
Contacts
Primary ContactMichael B Gill
Outcome results
None listed