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临床试验/NCT04275830
NCT04275830已完成不适用

The Effects of Heart Rate Variability Biofeedback Training on Hematopoietic Cell Transplantation Patients

Arizona State University2 个研究点 分布在 1 个国家目标入组 18 人开始时间: 2020年2月4日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
18
试验地点
2
主要终点
Changes from Baseline Heart Rate Variability (HRV and coherence scores) at 2 weeks

研究概览

简要总结

Patients undergoing hematopoietic stem cell transplantation (HCT) often continue to experience anxiety, depression, isolation, and other psychosocial distress due to the severe nature of the transplant experience. Storytelling interventions that provide an opportunity for emotional disclosure have shown preliminary efficacy to alleviate psychosocial distress and improve emotion regulation during health challenges. Not only are these changes observed in response to such interventions, but they can also be directly strengthened with HRV biofeedback (HRVB) training, a device-driven breath pacing practice that uses colored light signals to provide feedback to increase vagal tone and improve emotional responses and sleep quality by regulating negative affect and stress. This randomized controlled trial will explore the effects of HRV biofeedback (HRVB) training combined with a digital storytelling intervention and changes in psychosocial distress with a modified waitlist control in a population of Hematopoietic cell transplantation (HCT) patients.

详细描述

This randomized controlled trial will explore the effects of an HRV biofeedback (HRVB) training session with a modified waitlist control in a population of Hematopoietic cell transplantation (HCT) patients. We will secondarily explore effects of a brief storytelling intervention, with or without the prior HRVB training. Two group of 10 HCT patients over the age of 18 will be recruited and enrolled into the study. The time of participating in this study will be 2-week proposed activities from the time of enrollment to completion. Specific participation will include baseline data collection (about 30 minutes), HRVB training session (30 minutes), watching and discussing stories (15 min for each week= 30 minutes) and one final data collection (about 30 minutes) at the end. For HRVB group, participants will be instructed to practice their HRV biofeedback skills at home for 10 minutes each day for a two-week period (about 140 minutes). Lab visit is required only twice for baseline data collection and final data collection. Other works will be via internet.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
Double (Participant, Outcomes Assessor)

入排标准

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

入选标准

  • age 18 or older
  • recently underwent Hematopoietic cell transplantation (HCT) (within 3 months after hospital discharge)
  • must be able to speak, read, and write in English
  • access to a working phone and e-mail account
  • have a smart phone

排除标准

  • cognitive impairment that prohibits completion of study assessment visual or hearing impairment
  • other (e.g., provider non-approval or logistical constraints such as patient moving out of town)

结局指标

主要结局

Changes from Baseline Heart Rate Variability (HRV and coherence scores) at 2 weeks

时间窗: Baseline (T1), 2 weeks after (T2)

The Emwave Pro Plus device from HeartMath will be used to collect HRV data and heart rate using a 3-minutes "neutral" protocol (we call "waiting at the bus stop" implying that no particular intent for breath or mindful state is to be evoked) to understand the benefits of DS+ HRVB. In addition, HRV measures will be obtained for the 1-minute paced breathing period to understand the effects of paced breathing on HRV. The following precautions will be provided as instructions to participants prior to data collection: no coffee, tea, or caffeinated drinks such as energizing drinks in the 2 hours before the data collection, and no alcohol consumption during 24 hours prior to the data collection.

次要结局

  • Changes from Baseline Profile of Mood States (POMS) short version (Psychological Distress) at 2 weeks(Baseline (T1), 2 weeks after (T2))

研究者

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

Wonsun (Sunny) Kim, Ph.D

Assistant professor

Arizona State University

研究点 (2)

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