Dementia Clinical Trials: A Study on the Clinical Trial Participation of Dementia Patients
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Dementia
- Sponsor
- Power Life Sciences Inc.
- Enrollment
- 500
- Primary Endpoint
- Number of dementia patients who remain in clinical trial until completion.
- Status
- Not yet recruiting
- Last Updated
- 2 years ago
Overview
Brief Summary
This research aims to collect comprehensive data on the clinical trial experience of dementia patients. Its goal is to identify the factors that limit patients' ability to join or complete a trial successfully. Clinical trial participation often favors specific demographic groups, and limited research exists on the impact of trial attributes on participation. Therefore, this study aims to analyze data from various demographic groups and identify any recurring trends that could provide valuable insights for future dementia patients.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Ability to provide written informed consent obtained prior to participation in the study and any related procedures being performed.
- •Participant has a diagnosis of dementia.
- •Willing and able to comply with scheduled visits, treatment schedule, laboratory tests and other requirements of the study.
Exclusion Criteria
- •Pregnant or lactating woman
- •Enrolled in another research study
- •Any mental or medical condition that prevents the patient from giving informed consent or participating in the trial
Outcomes
Primary Outcomes
Number of dementia patients who remain in clinical trial until completion.
Time Frame: 12 months
Rate of patients who decide to enroll in a dementia clinical study.
Time Frame: 3 months