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Effectiveness of a Sound Bowl Meditation on Caregiver Stress and Anxiety

3 giugno 2026 aggiornato da: Beth Steinberg, Ohio State University

Effectiveness of a Sound Bowl Meditation on Caregiver Stress and Anxiety: A Pilot Study

Being a primary caregiver for a family member or friend can be physically and emotionally demanding leaving little time for the unpaid caregiver's professional pursuits, personal appointments, and self-care. Primary caregivers are often overwhelmed, and experience stress, anxiety, depression, and sleep disturbances. Passive activities that require no physical or mental exertion may provide support and can help improve overall well-being. Sounds from crystal sound bowls and other instruments combined with guided meditations have been found to promote relaxation and to reduce stress and anxiety. Participants can sit in a chair or lie on a yoga mat, supported by pillows and blankets, to enhance comfort and rest. Eye masks can also be used to minimize light and promote peacefulness. The purpose of this study is to assess if a weekly Sound Bowl Meditation, offered over the course of 6 weeks and provided by a certified Sound Bowl practitioner, can help decrease caregiver stress and anxiety related to the role as a primary caregiver.

Panoramica dello studio

Stato

Non ancora reclutamento

Condizioni

Intervento / Trattamento

Descrizione dettagliata

Over the past 10 years, the number of adults who provide essential in-home care for family members has increased by 50%. These family caregivers are often spouses or partners, adult children, siblings, parents, or other individuals within the patient's social network. Currently in the U.S., more than 42 million family members serve as primary caregivers for chronically ill and/or disabled adults or children, providing all physical care, symptom management, and psychosocial support. With little to no formal training, almost half of these family caregivers provide high-intensity medical care that involves complex medication administration, patient transfers and mobility assistance, and management of medical equipment. As the aging U.S. population increases, more individuals will need care and assistance while rising healthcare costs will make professional care, offered at home or within a facility, less accessible and less affordable. While education and skills training related to management of the family member's medical needs and safety for the caregiver are essential, regular interventions that can improve resilience, provide intellectual stimulation, promote social connection and relaxation are necessary to counter the negative effects of caregiving.

Sound medicine is a relatively new name for sound interventions that can elicit happiness, contentment, and relaxation. Sound interventions encompass musical and non-musical sounds, such as nature sounds and calming voices. Exposure to these sounds have shown reduced stress and improved well-being. Sound healing has been in existence for centuries and has been used in a variety of cultures as an integral part of life events and celebrations. While any instruments that produce a beat or melody can be used in sound healing, sound bowls, also called singing bowls, can produce frequencies that resonate within the human body to promote deep relaxation and an improved sense of well-being. Although the mechanism of effect is not well understood, the binaural beats and vibrations emitted by the sound bowls may interact with the energy field surrounding the human body. The beat frequency of the sound bowls mirrors the theta wave region of the brain which increases in the relaxed meditation state. The facilitation of more meditative state through exposure to sound bowl interventions has shown improvements in anxiety, depression, fatigue, and mood, as well as physiological improvements in blood pressure, heart rate, respiratory rate, peripheral oxygen saturation and positive electroencephalographic changes.

Supportive interventions for family caregivers should optimally provide brief periods of respite without requiring physical or mental exertion to perform. Participating or receiving a sound bowl intervention is passive and has no reported negative side effects. Given the gap in the literature related to the effects of sound bowl interventions for family caregivers, and the physical, mental, and emotional stressors inherent in the caregiving role, the evaluation of benefits for this low cost, low technology invention is practical and needed.

The purpose of this pilot study is to evaluate the effectiveness of a 6-week sound bowl meditation intervention on caregiver perceived stress and anxiety. Results from this pilot study will be used to assess feasibility of the study protocol and inform a future, larger study.

Due to the prevalence of caregiver perceived stress and anxiety, the investigators hypothesize that a sound bowl meditation intervention, offered weekly over the course of 6 weeks, will reduce caregiver perceived stress and anxiety.

Tipo di studio

Interventistico

Iscrizione (Stimato)

40

Fase

  • Non applicabile

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

Backup dei contatti dello studio

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Adulto
  • Adulto più anziano

Accetta volontari sani

No

Descrizione

Inclusion Criteria:

  1. Adults age 18 years and older
  2. Primary, unpaid caregiver of a family member (spouse, sibling, parent, child, etc.) or an unrelated adult (friend) who is chronically ill and/or disabled
  3. Primary, unpaid caregiver has provided care to family member or an unrelated adult for a minimum of six months
  4. Normal hearing capacity with or without corrective hearing aids
  5. Availability and willingness to participate in the six week sound bowl meditation intervention
  6. Access to a smartphone or personal electronic tablet with adequate WiFi access and a personal email
  7. Willingness and ability to download the MyCap app to complete study surveys

Exclusion Criteria:

  1. Professional and/or paid caregivers
  2. Inability to read and/or understand English (consent, study instructions, and questionnaires in English)

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Terapia di supporto
  • Assegnazione: N / A
  • Modello interventistico: Assegnazione di gruppo singolo
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: Intervention Group
Intervention Group will receive a 6-week (1-60 minute session weekly) sound bowl meditation in a community, group setting.
The study intervention is a sound bowl meditation, offered weekly (same day and same time of day) for six weeks; each session will be 60 minutes in length. The sound bowl meditation will include the use of a Reem drum, Tingsha bells (small cymbals used to induce relaxation, reduce stress, and restore energetic balance), and eight crystal sound bowls. Participants will be fully clothed and will be able to sit in a chair or lie on a yoga mat with yoga props used for comfort. The sound bowl meditation will be provided by certified Sound Bowl Practitioners from the OSU Wexner Medical Center who regularly provide these interventions in the community.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Generalized Anxiety Disorder-7
Lasso di tempo: At baseline and at the end of the 6-week intervention.
The GAD-7 is a self-report measure of the presence and severity of anxiety symptoms over the past two weeks. Each of the 7 questions are scored from 0 to 3; (0) "not at all", (1) "several days", (2) "more than half the days", and (3) "nearly every day". Scale scores range from 0 to 21 with a score of 0 to 4 indicating minimal anxiety, 5 to 9 indicating mild anxiety, 10 to 14 indicating moderate anxiety, and 15 to 21 indicating severe anxiety.
At baseline and at the end of the 6-week intervention.
Kingston Caregiver Stress Scale
Lasso di tempo: At baseline and at end of the 6-week intervention.
The 10-item KCSS is a self-report measure of the perceived stress experienced by community living lay caregivers who provide day-to-day care for a family member or acquaintance. The questions are divided into three sub-scales of stressors that include caregiving (7 questions), family issues (2 questions), and financial problems (1 question). The measure can be used to monitor changes in stress levels over time, as caregiving situations may change. For each of the 10 questions, the degree of stress is rated on a 1 to 5 scale that ranging from (1) Feeling Fine/No stress (Coping fine / no problems), (2) Some stress, (3) Moderate stress, (4) A lot of stress, to (5) Extreme Stress (feeling "at the end of rope", health at risk). The total score can range from 10 to 50 with higher scores indicating higher caregiver stress.
At baseline and at end of the 6-week intervention.

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Investigatori

  • Investigatore principale: Beth Steinberg, PhD, RN, The Ohio State Unversity

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Stimato)

1 ottobre 2026

Completamento primario (Stimato)

30 dicembre 2026

Completamento dello studio (Stimato)

1 giugno 2027

Date di iscrizione allo studio

Primo inviato

29 maggio 2026

Primo inviato che soddisfa i criteri di controllo qualità

29 maggio 2026

Primo Inserito (Effettivo)

4 giugno 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

5 giugno 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

3 giugno 2026

Ultimo verificato

1 maggio 2026

Maggiori informazioni

Termini relativi a questo studio

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

INDECISO

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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