- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT07581639
Comparison of Live and Virtual Music-based Interventions in Mitigating Stress
12. maj 2026 opdateret af: University of Pennsylvania
Comparison of Live and Virtual Music-based Interventions in Mitigating Stress: A Pilot Study
The purpose of this study is to learn if virtual music therapy with active engagement components leads to the same benefits as traditional live music therapy in mitigating stress in older adults.
This study aims to compare live and virtual music interventions among older adults with cognitive impairment living in assisted living facilities.
Studieoversigt
Status
Afsluttet
Betingelser
Intervention / Behandling
Undersøgelsestype
Interventionel
Tilmelding (Faktiske)
32
Fase
- Ikke anvendelig
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
-
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Pennsylvania
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Berwyn, Pennsylvania, Forenede Stater, 19312
- Conestoga High School
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Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
- Ældre voksen
Tager imod sunde frivillige
Ingen
Beskrivelse
Inclusion Criteria:
- Lives in included assisted living facility
- 65 years or older
- Able to provide informed consent
- Able to hear music
- Able to see a computer screen
- Able to speak
Exclusion Criteria:
- Does not live in included assisted living facility
- Younger than 65 years
- Unable to provide informed consent
- Unable to hear music
- Unable to see a computer screen
- Unable to speak
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Randomiseret
- Interventionel model: Crossover opgave
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
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Aktiv komparator: Live music therapy
The live music intervention was presented in the activities room of each senior center and included a classical violin for the performer (a classically trained violinist with experience arranging and playing pop music), a second violin for participant engagement, and a computer speaker for digital sound output (Dell, Inc.).
The live music intervention sessions included multiple active engagement components, such as music adjustment (e.g., lowering the tempo, changing to an upbeat piece) to match participants' apparent mood, verbal interaction, physical engagement (e.g., encouraging dancing, on-beat clapping), and singing along.
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The live music intervention was presented in the activities room of each senior center and included a classical violin for the performer (a classically trained violinist with experience arranging and playing pop music), a second violin for participant engagement, and a computer speaker for digital sound output (Dell, Inc.).
The live music intervention sessions included multiple active engagement components, such as music adjustment (e.g., lowering the tempo, changing to an upbeat piece) to match participants' apparent mood, verbal interaction, physical engagement (e.g., encouraging dancing, on-beat clapping), and singing along.
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Eksperimentel: Virtual music therapy
The virtual intervention followed identical procedures as the live intervention and involved similar active engagement components, with the music being delivered to the same cohort via video conference (Zoom Communications, Inc.).
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The virtual intervention followed identical procedures as the live intervention and involved similar active engagement components, with the music being delivered to the same cohort via video conference (Zoom Communications, Inc.).
In both live and virtual sessions, the performer showed identical levels of engagement and adjustment.
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Heart rate (HR)
Tidsramme: Baseline (15 minutes before the music intervention session) and follow-up (15 minutes after the music intervention session was completed)
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Registered nurses at each assisted living facility measured and recorded each participant's heart rate (HR) using an oxygen saturation monitor (Oxiline, Inc.).
The monitor was placed on each participants' finger and the heart rate was recorded for a 1-minute interval 15 minutes before and after each music-based session.
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Baseline (15 minutes before the music intervention session) and follow-up (15 minutes after the music intervention session was completed)
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Systolic blood pressure
Tidsramme: Baseline (15 minutes before the music intervention session) and follow-up (15 minutes after the music intervention session was completed)
|
Systolic blood pressure was measured using a sphygmomanometer (Curaplex, Inc.) immediately after the heart rate measurement
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Baseline (15 minutes before the music intervention session) and follow-up (15 minutes after the music intervention session was completed)
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Self-reported stress levels
Tidsramme: Baseline (15 minutes before the music intervention session) and follow-up (15 minutes after the music intervention session was completed)
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The self-reported stress survey was adapted and modified from Levenstein et al. (1993), with question wording modified to reduce the reading level.
The stress-assessment survey was condensed to a total of 10 questions, each rated on a 4-level Likert scale from strongly disagree (0) to strongly agree (3).
To maintain consistency, the rating on 4 items indicating lack of stress was reversed, so that 0 corresponded to 3 points.
The total score was calculated by adding the individual scores for each question (score range, 0 to 30, where a higher rating corresponds to greater stress).
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Baseline (15 minutes before the music intervention session) and follow-up (15 minutes after the music intervention session was completed)
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Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Samarbejdspartnere
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart (Faktiske)
1. august 2025
Primær færdiggørelse (Faktiske)
27. september 2025
Studieafslutning (Faktiske)
27. september 2025
Datoer for studieregistrering
Først indsendt
27. april 2026
Først indsendt, der opfyldte QC-kriterier
5. maj 2026
Først opslået (Faktiske)
12. maj 2026
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
15. maj 2026
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
12. maj 2026
Sidst verificeret
1. maj 2026
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- 01082025
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
INGEN
IPD-planbeskrivelse
Informed consent to share individual participant data was not obtained.
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
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