跳至主要内容
临床试验/NCT03952767
NCT03952767已完成不适用

The STEPP Study: Sensors To Evaluate Physical Performance

UNC Lineberger Comprehensive Cancer Center2 个研究点 分布在 1 个国家目标入组 63 人开始时间: 2019年4月24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
63
试验地点
2
主要终点
Amount of mean steps per day recorded at home

研究概览

简要总结

This study assesses the association between digital functional measures of physical and patient-reported standard onocological assessments, like Karnofsky Performance Score (KPS).

详细描述

This study assess the association between digital functional measures from physical monitoring devices (devices like a watch tracking steps, a heart rate monitor) and patient-reported standard oncological assessments. The study will also test the feasibility of obtaining the measures in clinic and at home from the monitoring devices in participants with cancer. Participants will be asked to spend 1 hour in clinic performing simple tasks such as walking and standing with 7 digital devices recording movement data. The participants will also be asked to fill out survey data regarding their health. At-home data will be collected for 14 days. During this time participants will wear a watch to collect movement and step data, and a lumbar belt to collect movement data.

Primary Objective:

  1. Assess the association of 5 main digital physical functional measures (mean steps per day, mean sedentary activity time, light activity time, moderate activity time, and vigorous activity time (in minutes) per day) recorded at home with patient-reported standard oncological assessment (e.g. KPS)

研究设计

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

入排标准

年龄范围
18 Years 至 99 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • All genders aged ≥ 18 years of age
  • Patients being seen at UNCCH for treatment of cancer.
  • English-speakers
  • Able to understand and cooperate with study procedures.
  • Patients with solid tumors or hematological malignancies, and self-reported KPS ≤70 to ≥
  • Signed and dated informed consent and HIPPA.

排除标准

  • Subjects using investigational/experimental products.
  • Has dementia, altered mental status, or any psychiatric or co-morbid condition prohibiting the understanding or rending of informed consent.
  • Unable or unwilling to complete physical performance assessments including the at-home wearable device for 14 days.
  • Unable to speak English.
  • Subjects who report any other medical condition, recreational substance use, or medication use which would prevent them from completing study tasks or impair the providing of informed consent.
  • Subjects who are allergic to silicone or adhesives. Subjects with cardiac pacemakers, electronic pumps or any other implanted medical devices.

结局指标

主要结局

Amount of mean steps per day recorded at home

时间窗: 18 months

At-home record of mean steps per day

Amount of Light activity time recorded at home

时间窗: 18 months

At-home record of minutes per day of light activity time per day

Amount of moderate activity time recorded at home

时间窗: 18 months

At-home record of minutes per day of moderate activity time

Amount of vigorous activity time recorded at home

时间窗: 18 months

At-home record of minutes per day of vigorous activity time

Amount of mean sedentary activity time recorded at home

时间窗: 18 months

At-home record of minutes per day of mean sedentary activity time

Self-Reported Karnofsky Performance Score (KPS)

时间窗: 18 months

The validated 1 question Self-reported Karnofsky Performance Score (KPS) score 0 to 100 will be measured. Scores closer to 100 indicate high performance of the patient

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

Loading locations...

相似试验