NCT05811858Not yet recruitingNot Applicable
Analyzing Factors Impacting Patient Involvement in Osteoarthritis Clinical Research
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Not yet recruiting
- Sponsor
- Power Life Sciences Inc.
- Enrollment
- 500
- Primary Endpoint
- Rate of patients who decide to enroll in an osteoarthritis clinical study.
Study Overview
Brief Summary
Clinical research participation percentages haven't always been fully representative of a given demographic.
The goal is to find out which aspects of a clinical trial may make it more difficult for patients to take part or see it through.
The data will be evaluated through different demographic lenses and identify trends that could help improve the experience of future osteoarthritis patients during clinical study.
Study Design
- Study Type
- Observational
- Observational Model
- Case Crossover
- Time Perspective
- Prospective
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Aged ≥ 18 years old and ability to provide written informed consent obtained prior to participation in the study and any related procedures being performed.
- •Participant has a diagnosis of osteoarthritis.
- •Willing and able to comply with scheduled visits, treatment schedule, laboratory tests and other requirements of the study.
Exclusion Criteria
- •Patients with any significant history of non-compliance to medical regimens or with inability to grant a reliable informed consent.
- •Pregnant or lactating woman
- •Known medical condition that, in the investigator's opinion, would increase the risk associated with study participation or study drug(s) administration or interfere with the interpretation of safety results
Outcomes
Primary Outcomes
Rate of patients who decide to enroll in an osteoarthritis clinical study.
Time Frame: 3 months
Number of osteoarthritis patients who remain in clinical trial until completion.
Time Frame: 12 months
Secondary Outcomes
No secondary outcomes reported
Investigators
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