Recruiting NA Cognitive Decline

New treatment option for Cognitive Decline

Official title Effects of Real vs. Soundless Acoustic Stimulation During Deep Sleep on Brain Activity, Memory, and Blood Biomarkers in Older Adults (60-85) With Mild Memory Impairment

ClinicalTrials.gov ID: NCT06669546

What this study is testing

What it's testing
This study aims to explore a non-invasive way to improve memory and slow cognitive decline in older adults by enhancing sleep quality. Dementia, a leading cause of death worldwide, is often associated with disturbed sleep, particularly the loss of deep, slow-wave sleep (SWS).

A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.

Who can take part

Ages 60 to 85

You may be able to join if

  • Written informed consent
  • Age between 60 and 85 years
  • Cognitive impairment (subjective and/or MoCA between 23-26)
  • Native German speakers or comparably fluent
  • Normal or corrected-to-normal vision.

You likely can't join if

  • Insomnia assessed by the Regensburg Insomnia Scale (RIS; Crönlein et al., 2013)
  • Restless leg syndrome assessed by questions concerning typical symptoms.
  • Sleep apnoea assessed by the Berlin Questionnaire (BQ; Netzer et al., 1999)
  • Severely irregular sleep patterns assessed by the RIS and the Pittsburgh sleep quality index (PSQI; Buysse et al., 1989)
  • Symptoms of depression (Geriatric Depression Scale (GDS; Yesavage et al., 1982) ≥ 5)
  • History of untreated severe neurological and psychiatric diseases
See the full eligibility criteria
Who can join
  • Written informed consent
  • Age between 60 and 85 years
  • Cognitive impairment (subjective and/or MoCA between 23-26)
  • Native German speakers or comparably fluent
  • Normal or corrected-to-normal vision.
  • Intact hearing
  • A close cohabitant (partner/sibling) should be present to support participants in using study materials/devices.
What rules you out
  • Insomnia assessed by the Regensburg Insomnia Scale (RIS; Crönlein et al., 2013)
  • Restless leg syndrome assessed by questions concerning typical symptoms.
  • Sleep apnoea assessed by the Berlin Questionnaire (BQ; Netzer et al., 1999)
  • Severely irregular sleep patterns assessed by the RIS and the Pittsburgh sleep quality index (PSQI; Buysse et al., 1989)
  • Symptoms of depression (Geriatric Depression Scale (GDS; Yesavage et al., 1982) ≥ 5)
  • History of untreated severe neurological and psychiatric diseases
  • Alcohol or substance abuse
  • Use of medication acting on the central nervous system

The study team makes the final eligibility decision.

Where it's taking place

  • Bern, Switzerland

Questions & answers

Do participants get paid in this trial?

This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.

Is it free to join, and do I need insurance?

Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.

How long does this study last?

The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.

Who can join this trial?

This study is enrolling all sexes, 60 years to 85 years. The study team makes the final eligibility decision.

Where is this trial taking place?

Study sites include Bern, Switzerland. Enter your location above to see the nearest site and check your eligibility.

Explore other conditions

BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.