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临床试验/NCT05161260
NCT05161260已完成不适用

Pilot Study of Group Video Yogic Breathing App in Breast Cancer Survivors

Medical University of South Carolina1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2021年11月17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
40
试验地点
1
主要终点
Total Practice Time as Assessed in Minutes Within the Study Application.

研究概览

简要总结

Cancer survivorship is associated with many long-term chronic health issues that arise as a result of cancer treatment protocols. Non-pharmacological lifestyle and mind-body interventions have been shown to be effective and critical components of a total-health strategy for cancer survivors. PranaScience Institute seeks to develop and test a novel group video app for home-based delivery of a Yogic Breathing intervention that reduces symptoms of cancer treatment survival and supports total-health.

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
Single (Participant)

入排标准

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

入选标准

  • Age 18 years or older, willing to provide informed consent.
  • Diagnosis of Stage 0-III breast cancer.
  • Completion of radiation therapy within the last 6 months.
  • ECOG performance status of 0-3 during cancer treatment.
  • Orally expressed visual and auditory acuity adequate for filling out all study forms and participating in telephone interviews and internet-based group video applications.
  • Access to telephone and internet-connected computer or mobile phone.

排除标准

  • Subject is unwilling or unable to comply with any of the study procedures.
  • Orally expressed dependence on alcohol or drugs.

研究组 & 干预措施

Yoga Breathing (YB)

Experimental

A first production version of a mobile application that guides users through proscribed yoga breathing exercises.

干预措施: Yoga Breathing (Behavioral)

Attention Control

Experimental

A first production version of a mobile application that guides users through an attention control activity, presented as methods for mindfulness.

干预措施: Attention Control (Behavioral)

结局指标

主要结局

Total Practice Time as Assessed in Minutes Within the Study Application.

时间窗: 12 weeks

Adherence will be evaluated by assessing total practice times by length in minutes.

Practice Frequency as a Measure of Adherence

时间窗: 12 weeks

Adherence is assessed by quantifying the number of completed app-based practice sessions relative to the total number of available sessions over 12 weeks. Each practice session is defined as a 10-minute, app-timed exercise, automatically logged in the mobile application's backend (including both individual and group sessions). Adherence is operationalized as: Practice Frequency = total number of completed sessions Practice Proportion = completed sessions ÷ total possible sessions (180 sessions maximum; 3 sessions/day × 5 days/week × 12 weeks). Both metrics are captured automatically by the app, which records each timed session as a completed practice. Higher values indicate greater adherence.

Participants' Symptom Management as Measured by the System Usability Scale.

时间窗: 12 weeks

Acceptability measures the participant's symptom management throughout the study duration. This is measured using The System Usability Scale (SUS) questionnaire, a 10 item questionnaire with 5 response options ranging from 'Strong Agree' to 'Strong Disagree'. The questionnaire will be administered at the end of 12 weeks to measure participants' acceptability of the study application. The acceptability is defined as a value of at least 68% in System Usability Scale. The values 0.6 and 0.2 represent 60% and 20% respectively. The higher percentage indicates greater system usability (meaning acceptability) of the app.

次要结局

  • Change in Perceived Stress (Perceived Stress Scale-10)(12 weeks)
  • Change in Depression Symptoms (Depression Scale)(12 weeks)
  • Change in Symptom Burden (MD Anderson Symptom Inventory)(12 weeks)

研究者

申办方类型
Other
责任方
Sponsor
主要研究者

Sundar Balasubramanian

Principal Investigator, Founder, Owner

PranaScience Institute LLC

研究点 (1)

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