跳至主要内容
临床试验/NCT07672925
NCT07672925招募中不适用

Feasibility of Using a Meditation App in Adults With Anxiety Disorder

National University of Natural Medicine1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2025年10月15日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
40
试验地点
1
主要终点
Feasibility of the FlowMD mobile app

研究概览

简要总结

The goal of this clinical trial is to learn if the FlowMD mobile app is feasible to be used to manage mild anxiety in adults. It will also learn if the app is effective at managing anxiety in adults.

Participants will:

Use the FlowMD app daily to complete a 1-5 minute guided breathwork session over the course of 4 weeks.

Complete surveys at the beginning, midpoint, and end of the study to measure anxiety levels and usability of the app.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Other
盲法
None

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Are 18-65 years old
  • Have an anxiety disorder
  • Have a smartphone
  • Able to download the FlowMD app
  • Willing to use the FlowMD meditation app for a daily 1-5 minute session for four consecutive weeks
  • Able to provide feedback on the experience using the app
  • Willing to participate in surveys to measure changes in anxiety levels

排除标准

  • Are undergoing significant changes in psychiatric medication or therapy
  • Have severe psychiatric conditions that might interfere with study participation (Schizophrenia, Bipolar Disorder, Major Depressive Disorder)

研究组 & 干预措施

Intervention

Active Comparator

Daily guided breathwork using the FlowMD mobile app

干预措施: Intervention (Other)

Control

No Intervention

Control Group with no Intervention

结局指标

主要结局

Feasibility of the FlowMD mobile app

时间窗: From enrollment to end of intervention at 4 weeks

Outcome measured using the Feasibility Survey with a Max Score of 32 indicating strong feasibility

次要结局

  • Generalized Anxiety Disorder-7 (GAD-7) Score(From Enrollment to the end of the intervention at 4 weeks)
  • Hamilton Anxiety Rating Scale (HAM-A) Score(From Enrollment to the end of the intervention at 4 weeks)
  • State-Trait Anxiety Inventory (STAI)(From Enrollment to the end of the intervention at 4 weeks)

研究者

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

Heather Zwickey

Principal Investigator

National University of Natural Medicine

研究点 (1)

Loading locations...

相似试验