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Navigating the Clinical Research Process for Mild Cognitive Impairment

P

Power Life Sciences

Status

Not yet enrolling

Conditions

Mild Cognitive Impairment

Study type

Observational

Funder types

Industry

Identifiers

NCT06207903
58428170

Details and patient eligibility

About

Participation in medical research usually favors a particular demographic group. But there is limited research available to explain what trial attributes affect the completion of these specific demographic groups.

This trial will admit a wide range of data on the clinical trial experience of mild cognitive impairment patients to determine which factors prevail in limiting a patient's ability to join or finish a trial.

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 future mild cognitive impairment patients.

Enrollment

500 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Confirmed diagnosis of mild cognitive impairment
  • Participant must be 18 years of age or older
  • Participant must be willing and able to comply with scheduled visits, treatment schedule, laboratory tests, and other requirements of the study.

Exclusion criteria

  • Pregnant or lactating woman
  • Participant is actively receiving study therapy in another
  • Inability to provide written informed consent

Trial design

Trial documents
1

Trial contacts and locations

1

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Central trial contact

Michael B Gill

Data sourced from clinicaltrials.gov

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