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A Controlled Study on Fighting Against Anxiety in Older People Through an Educational Audio Programme. (ECLIPSE)

4. november 2026 oppdatert av: Centre Hospitalier de Cannes Simone Veil

EXPLORATORY, PROSPECTIVE, MONO-CENTRIC, RANDOMISED, CONTROLLED, OPEN LABEL, STUDY EVALUATING BENEFITS OF A DIGITAL AUDIO PROGRAMME ON ANXIETY IN AGED CARE HOMES' RESIDENTS

In residential care homes for the elderly, safeguarding the mental and emotional health of aged people is a key factor in their well-being and the quality of care they receive. Among these disorders, anxiety plays a central role. Furthermore, in aged people, anxiety is frequently associated with other psychological and functional vulnerabilities, notably depression and sleep disorders, with which it frequently interacts. Taken together, these factors contribute to a cycle of emotional, cognitive and functional vulnerability that can impair the well-being of residents in care homes. In light of these challenges, non-pharmacological interventions (NPIs), which have the potential to reduce anxiety and depression and improve sleep, represent a particularly promising complementary approach and are attracting growing interest in the care of aged people living in care homes. The Simone Veil Gerontology Institute and Care Home of Cannes Hospital wishes to offer its residents a sound immersion programme as part of their standard care. The audio content is sourced from the SOMEO Life digital platform, an audio-guided application accessible via wireless headphones connected to a tablet or smartphone, allowing for individual or group use. This application offers pre-recorded sessions on relaxation, guided breathing and sophrology tailored to aged people living in care homes. In this context, this study aims to explore and evaluate, within a pragmatic and institutional framework, the benefits of an audio-guided sound immersion programme (SOMEO Life platform) on the current levels of anxiety among residents living in care homes. Depressive symptoms, sleep disorders and the use of anti-anxiety medication will also be assessed.

An exploratory, prospective, single-centre, randomised, controlled, open-label study evaluating the benefits of a digital audio programme on anxiety in elderly people in care homes is implemented. Forty patients will be recruited (twenty per groups) and followed-up during 3 months.

Primary objective is to determine whether adding an audio-guided sound immersion programme to standard care reduces the current level of anxiety (state anxiety) in patients in residential care homes for the elderly. Study endpoint is State-Trait Anxiety Inventory (STAI-Y), specifically the State Anxiety (Y-A) subscale.

Studieoversikt

Status

Har ikke rekruttert ennå

Studietype

Intervensjonell

Registrering (Antatt)

40

Fase

  • Ikke aktuelt

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiekontakt

Studiesteder

    • Alpes-maritime
      • Cannes, Alpes-maritime, Frankrike, 06400
        • Centre Hospitalier de Cannes Simone Veil
        • Ta kontakt med:
        • Hovedetterforsker:
          • Charlotte PREVENT, Psychologist

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

18 år og eldre (Voksen, Eldre voksen)

Tar imot friske frivillige

Nei

Kjønn som er kvalifisert for studier

Alle

Beskrivelse

Inclusion Criteria:

  • Residents who have been living in the care home for more than 2 months; · - A Mini Mental State Examination (MMSE) score of ≥ 20/30*, obtained in routine clinical practice within the 6 months prior to enrolment;
  • Patients with sufficient French language understanding, as assessed by the investigators
  • Patient's consent to participate in the study;
  • For patients under guardianship, curatorship or judicial protection, consent from the legal representative.
  • Social security scheme affiliation

Exclusion Criteria:

  • Patients with hearing loss who do not wear a hearing aid or whose hearing impairment prevents them from making effective use of the audio equipment;
  • Patients who, in the investigator's opinion, are unable to understand the objectives of the study or meet its criteria

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Annen
  • Tildeling: Randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Aktiv komparator: control group: standard programme

"Standard" programme usually available for patients: organised on a group basis: cognitive stimulation workshops, leisure activities (outings, shows or films), inter-generational workshops (meetings with children), inter-care home workshops (meetings with other residents), soft gym, craft or creative workshops, relaxation and sophrology workshops, and choral

"Standard" programme usually available for patients: organised on a group basis: cognitive stimulation workshops, leisure activities (outings, shows or films), inter-generational workshops (meetings with children), inter-care home workshops (meetings with other residents), soft gym, craft or creative workshops, relaxation and sophrology workshops, and choral

Andre navn:
  • Usual care programme
Eksperimentell: experimental group: digital audio programme
  • usual programme available for patients: organised on a group basis: cognitive stimulation workshops, leisure activities (outings, shows or films), inter-generational workshops (meetings with children), inter-care home workshops (meetings with other residents), soft gym, craft or creative workshops, relaxation and sophrology workshops, and choral
  • two Audio immersion workshops added to weekly usual programme

"Standard" programme usually available for patients: organised on a group basis: cognitive stimulation workshops, leisure activities (outings, shows or films), inter-generational workshops (meetings with children), inter-care home workshops (meetings with other residents), soft gym, craft or creative workshops, relaxation and sophrology workshops, and choral

Andre navn:
  • Usual care programme

A non-pharmaceutical, digital sound immersion solution designed to improve the wellbeing of elderly people in care homes. The app, developed by SOMEO Solutions, offers structured audio programmes incorporating verbal guidance and a soothing soundscape. The audio content can be accessed via a mobile device without the need to download an app, and the audio is played through wireless earphones or headphones connected to a transmitter The platform can be accessed via a QR code or a dedicated URL, without the need to download anything or create an account. Access is anonymous. The playback equipment can be standard headphones (or earphones) or a UHF wireless headphone kit - over-ear, closed-back, with individually adjustable volume, and compatible with hearing aids.

Andre navn:
  • group sound immersion workshop

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
State-Trait Anxiety Inventory (STAI-Y) A-section Scale
Tidsramme: From enrollment to the end of programme at 3months

State-Trait Anxiety Inventory (STAI-Y), in its State Anxiety (Y-A) section, measured at two timepoints:

  • baseline record (timepoint 1) at initiation visit V0 or first interventionnal visit V1
  • end of follow-up record (timepoint 2) at 3months post V1 Score range: [20-80]. outcome is the score difference: end of follow-up record minus baseline record
From enrollment to the end of programme at 3months

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Etterforskere

  • Hovedetterforsker: Charlotte PREVENT, Psychologist, Centre Hospitalier de Cannes Simone Veil

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Antatt)

2. januar 2027

Primær fullføring (Antatt)

2. juni 2028

Studiet fullført (Antatt)

31. desember 2028

Datoer for studieregistrering

Først innsendt

4. november 2026

Først innsendt som oppfylte QC-kriteriene

4. november 2026

Først lagt ut (Faktiske)

10. november 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

10. november 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

4. november 2026

Sist bekreftet

1. november 2026

Mer informasjon

Begreper knyttet til denne studien

Nøkkelord

Ytterligere relevante MeSH-vilkår

Andre studie-ID-numre

  • 2026-A01994-47
  • CHC-PI/2026-03 (Annen identifikator: Centre Hospitalier de Cannes Simone Veil)

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

UBESLUTTE

IPD-planbeskrivelse

data are own by CENTRE HOSPITALIER DE CANNES SIMONE VEIL, please contact sponsor for further information

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Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

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