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临床试验/NCT05727514
NCT05727514已完成不适用

A Trauma-Informed Music Composition Program Supporting Resilience in Individuals Hospitalized During the COVID-19 Pandemic

Brigham and Women's Hospital1 个研究点 分布在 1 个国家目标入组 14 人开始时间: 2021年4月22日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
14
试验地点
1
主要终点
New General Self-Efficacy Scale [NGSE]

研究概览

简要总结

This study explores the feasibility and acceptability of a music composition intervention to support resilience in survivors of serious illness hospitalized during the COVID-19 pandemic.

详细描述

This study explores the feasibility and acceptability of a music composition intervention to support resilience in survivors of serious illness hospitalized during the COVID-19 pandemic. The pandemic introduced widespread trauma for patients facing hospitalization. Therapeutic music interventions have demonstrated positive psychological effects, but none have explored the specific trauma-informed aspects of a composition-mentor program, as well as the specific impact of music composition on resilience-related traits.

Researchers implemented an adapted version of the New York Philharmonic Very Young Composers program (VYC): trained composer-mentors guide participants through four web-based sessions to elicit and develop participants' unique musical ideas into finished compositions. Participants are then invited to view a string quartet performance of their compositions. The Brief Resilience Scale [BRS] and New General Self-Efficacy Scale [NGSE] are administered pre-intervention, post-intervention, and post-performance.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Prevention
盲法
None

盲法说明

participants identity was not disclosed during the program

入排标准

年龄范围
18 Years 至 60 Years(Adult)
性别
All
接受健康志愿者
是

入选标准

  • •18 to 60 years of age
  • •Massachusetts residents
  • •exhibiting English fluency
  • •in care with an MGB provider
  • •admitted as an inpatient for at least 3 days to an MGB hospital between March 15, 2020 and July 21, 2022
  • •not hospitalized within the month before starting the study.

排除标准

  • •neuropsychiatric illness impeding participation in the study including suicidality, psychosis, active substance use, and dementia

研究组 & 干预措施

enrolled participants

Other

participation in 4-session music composition program with optional viewing of performance at the end

干预措施: music composition (Other)

结局指标

主要结局

New General Self-Efficacy Scale [NGSE]

时间窗: Data was collected at three time points over 5 months: Pre-Intervention (Baseline: upon enrollment), Post-Intervention (after the final intervention session), and Post-performance (after the final performance).

The New General Self-Efficacy (NGSE) scale evaluates one's perception of their overall ability to perform successfully in a variety of common scenarios by rating each item from 1-"Strongly Disagree" to 5-"Strongly Agree". Responses were scored by averaging the ratings across items. Min possible score: 1 Max possible score: 5 Min study score: 3.125 Max study score: 5.00 Higher scores mean a better outcome.

Post-musical performance program questionnaire

时间窗: Data was collected at one time point, within two weeks following the end of the music performance

Four questions designed for this study elicited open-ended feedback regarding the participant experience of listening to their music composition performed by professional musicians: (1) What was it like to hear your composition performed by professional musicians? (2) How did participating in this performance increase the impact of this program overall? (3) Does this program make you feel more confident about being able to be creative in the future? (4) Would you recommend attending the performance as part of this program to other survivors of serious illness?

Post-musical composition program questionnaire

时间窗: Data was collected at one time point, within one week following the final session of the music composition intervention

Four questions designed for this study elicited open-ended feedback regarding the participant experience of the program: (1) What did you enjoy about this program? (2) What did you find challenging about this program? (3) What did you learn about yourself through this program? (4) Would you recommend this program to other survivors of serious illness?

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Nomi Levy-Carrick, MD, MPHIL

Psychiatrist; Vice Chair, Clinical Program, Dept Psychiatry

Brigham and Women's Hospital

研究点 (1)

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