Allgemeine Informationen
  • Krankheitskategorie Demenz und Alzheimer (BASEC)
  • Studienphase N/A (ICTRP)
  • Rekrutierungsstatus Rekrutierung läuft (BASEC/ICTRP)
  • Studienstandort
    Bern
    (BASEC)
  • Studienverantwortliche Korian Wicki korian.wicki@unibe.ch (BASEC)
  • Datenquelle(n) BASEC: Import vom 08.01.2025 ICTRP: Import vom 12.04.2025
  • Letzte Aktualisierung 12.04.2025 02:00
HumRes66026 | SNCTP000006178 | BASEC2024-00409 | NCT06669546

Do soft sounds played during sleep have an impact on memory?

  • Krankheitskategorie Demenz und Alzheimer (BASEC)
  • Studienphase N/A (ICTRP)
  • Rekrutierungsstatus Rekrutierung läuft (BASEC/ICTRP)
  • Studienstandort
    Bern
    (BASEC)
  • Studienverantwortliche Korian Wicki korian.wicki@unibe.ch (BASEC)
  • Datenquelle(n) BASEC: Import vom 08.01.2025 ICTRP: Import vom 12.04.2025
  • Letzte Aktualisierung 12.04.2025 02:00

Zusammenfassung der Studie

Healthy sleep is important for health. In this study, we want to test individuals aged 60 to 85 with memory difficulties to find out how improved sleep affects memory and concentration tasks. For this study, participants will be invited to sleep at home for 8 weeks with a portable device, spread over a period of 3 months. This device allows for soft sounds to be played during the night while simultaneously measuring brain activity via electroencephalography (EEG). The sounds played are intended to have a positive impact on deep sleep. Before and after two 4-week intervention phases, blood samples will be taken to investigate metabolic products. At these times, participants will also solve cognitive tasks on-site at the University Clinic for Geriatric Psychiatry and Psychotherapy, UPD Bern. During the day, they will be invited to play memory games on a tablet app, which will help us measure memory performance.

(BASEC)

Untersuchte Intervention

Acoustic stimulation during deep sleep

(BASEC)

Untersuchte Krankheit(en)

Dementia, Alzheimer, memory difficulties

(BASEC)

Kriterien zur Teilnahme
- Age between 60 and 85 - Mild memory difficulties - Fluent German language skills (BASEC)

Ausschlusskriterien
- Severe sleep problems or use of sleep medications - Hearing or uncorrected vision impairment - Mental or neurological disorder - Living alone (BASEC)

Studienstandort

Bern

(BASEC)

Switzerland (ICTRP)

Sponsor

nicht verfügbar

Kontakt für weitere Auskünfte zur Studie

Kontaktperson Schweiz

Korian Wicki

+41 31 932 84 84

korian.wicki@unibe.ch

(BASEC)

Allgemeine Auskünfte

University Hospital of Old Age Psychiatry and Psychotherapy, University of Bern, 3000 Bern, Switzerland,

+41 (0)58 630 95 02;+ 41 (0)58 630 68 77

korian.wicki@unibe.ch

(ICTRP)

Allgemeine Auskünfte

University Hospital of Old Age Psychiatry and Psychotherapy, University of Bern, 3000 Bern, Switzerland

+41 (0)58 630 95 02+ 41 (0)58 630 68 77

korian.wicki@unibe.ch

(ICTRP)

Wissenschaftliche Auskünfte

University Hospital of Old Age Psychiatry and Psychotherapy, University of Bern, 3000 Bern, Switzerland,

+41 (0)58 630 95 02;+ 41 (0)58 630 68 77

korian.wicki@unibe.ch

(ICTRP)

Name der bewilligenden Ethikkommission (bei multizentrischen Studien nur die Leitkommission)

Ethikkommission Bern

(BASEC)

Datum der Bewilligung durch die Ethikkommission

30.09.2024

(BASEC)


ICTRP Studien-ID
NCT06669546 (ICTRP)

Offizieller Titel (Genehmigt von der Ethikkommission)
nicht verfügbar

Wissenschaftlicher Titel
Preventing Cognitive Decline Using Portable, Non-invasive Sleep Enhancement (ICTRP)

Öffentlicher Titel
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 (ICTRP)

Untersuchte Krankheit(en)
Cognitive DeclineAlzheimer DiseaseSubjective Cognitive Decline (SCD)Mild Cognitive Impairment (MCI)Cognitive Impairment, Mild (ICTRP)

Untersuchte Intervention
Other: Phase-locked auditory stimulation (PLAS)Other: Sham Phase-Locked Auditory Stimulation (ICTRP)

Studientyp
Interventional (ICTRP)

Studiendesign
Allocation: Randomized. Intervention model: Crossover Assignment. Primary purpose: Prevention. Masking: Single (Participant). (ICTRP)

Ein-/Ausschlusskriterien
Inclusion Criteria:

- 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.

Exclusion Criteria:

- Insomnia assessed by the Regensburg Insomnia Scale (RIS Crnlein 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 (ICTRP)

nicht verfügbar

Primäre und sekundäre Endpunkte
Episodic memory performance differences (between and within subject) according to the experimental condition (ICTRP)

Electrophysiological Response - Event-Related Potentials (ERPs);Electrophysiological Response - Power, Number, and Amplitude of Slow Oscillations (SO) and Spindles;Electrophysiological Response - Coupling of Slow Oscillations and Sleep Spindles;Amyloid-Beta Response;Electrophysiology - Brain Age Estimation (ICTRP)

Registrierungsdatum
29.10.2024 (ICTRP)

Einschluss des ersten Teilnehmers
nicht verfügbar

Sekundäre Sponsoren
University of Zurich;Amsterdam University Medical Centers (UMC), Location Academic Medical Center (AMC) (ICTRP)

Weitere Kontakte
Marc A Z?st, PhD;Marc A Z?st, PhD;Korian Wicki, Master, marc.a.zuest@unibe.ch; korian.wicki@unibe.ch, +41 (0)58 630 95 02;+ 41 (0)58 630 68 77, University Hospital of Old Age Psychiatry and Psychotherapy, University of Bern, 3000 Bern, Switzerland, (ICTRP)

Sekundäre IDs
215333, 2024-00409 (ICTRP)

Angaben zur Verfügbarkeit von individuellen Teilnehmerdaten
nicht verfügbar

Weitere Informationen zur Studie
https://clinicaltrials.gov/ct2/show/NCT06669546 (ICTRP)

Ergebnisse der Studie

Zusammenfassung der Ergebnisse

nicht verfügbar

Link zu den Ergebnissen im Primärregister

nicht verfügbar