Appraising Clinical Trial Experiences of Patients With Insomnia

Starting soon

Conditions studied: Insomnia

In brief

Medical 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 insomnia patients during clinical study.

Key facts

Study ID

NCT05978271

Run by

Power Life Sciences Inc.

People needed

500

Starts

2024-08-01

Expected to finish

2026-08-01

Last updated by the study team

2023-08-07

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• 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 insomnia.
• Willing and able to comply with scheduled visits, treatment schedule, laboratory tests and other requirements of the study.

You may not qualify if…

• Patients with any significant history of non-compliance to medical regimens or with inability to grant a reliable informed consent.
• 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.
• Pregnant or lactating woman

Where it is running

• Power Life Sciences — San Francisco, California, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.