Understanding Clinical Research for Mild Cognitive Impairment

This study is looking at how people with Mild Cognitive Impairment (MCI) experience clinical research. It aims to understand what helps or hinders someone from joining and completing a study. Researchers will collect a lot of information about participants' experiences to see if certain factors or demographic groups (like age or background) affect participation. The goal is to learn how to make future studies better for people with MCI. You can join if you are 18 or older with a confirmed MCI diagnosis and are willing to follow study requirements. The study is currently unclear on its recruitment status.

Study design
This is an observational study planning to enroll 500 participants. It will track how many patients decide to enroll in a study (measured at 3 months) and how many complete it (measured at 12 months).
What's involved
You must be willing and able to comply with scheduled visits, laboratory tests, and other requirements of the study.
Compensation
Not stated in the trial record.
Follow-up
Participants will be followed to see if they complete a clinical study, measured at 12 months.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT06207903

Navigating the Clinical Research Process for Mild Cognitive Impairment

Not Yet Recruiting
Not specifiedAges 18+Observational
Power Life Sciences Inc.
~500 participants
Updated 2024-01-17 on ClinicalTrials.gov

At a glance

Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Rate of patients who decide to enroll in a mild cognitive impairment clinical research.
Measured over 3 months
+1 more outcome measured
Mild Cognitive Impairment

NCT06207903

Where you'd take part

This study runs at 1 site. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.

  • Power Life Sciences

    San Francisco, Californiastudy coordinator listed

Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.

  • Michael B Gill · STUDY_DIRECTOR · Power Life Sciences Inc.

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Eligibility criteria

Inclusion

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

Pregnant or lactating woman
Participant is actively receiving study therapy in another
Inability to provide written informed consent
  • Rate of patients who decide to enroll in a mild cognitive impairment clinical research.3 months
  • Number of mild cognitive impairment study participants who remain in clinical study until completion.12 months