跳至主要内容
临床试验/NCT05021185
NCT05021185已完成不适用

Interactive Mobile Doctor (iMD) to Promote Tobacco Cessation Among Cancer Patients

University of California, San Francisco2 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2022年11月15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
30
试验地点
2
主要终点
Proportion of iMD participants who complete 2 or more sessions

研究概览

简要总结

The proposed pilot study aims to develop and test a patient video educational tool, an interactive Mobile Doctor (iMD), that can be integrated in radiation oncology setting to effectively engage cancer patients receiving treatment at University of California, San Francisco (UCSF) to facilitate smoking cessation and maintaining smoking abstinence in the context of their radiation treatment.

This study is the first to address tobacco use among can patients receiving radiation therapy that targets both tobacco cessation (current users) and maintaining abstinence (former users who have recently quit).

详细描述

The interactive Mobile Doctor (iMD) is an interactive video educational program that delivers tailored messages in response to participants' input, generates a summary report providing tobacco use status and cessation resources and solicits participants' interest in receiving referral or information to tobacco cessation resources.

PRIMARY OBJECTIVE:

I. To assess the feasibility and acceptability of the interactive Mobile Doctor (iMD), an interactive patient education tool, utilizing patient-centered and interactive technology approaches to target cancer patients who report using tobacco within the past 12 months and who are receiving or planning to receive radiation therapy for cancer.

SECONDARY OBJECTIVES:

I. To assess preliminary efficacy of iMD on tobacco abstinence when compared to the control (assessment + resource information only).

研究设计

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

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 order
  • Ability to understand study procedures and to comply with them for the entire length of the study.
  • Ability of individual or legal guardian/representative to understand a written informed consent document, and the willingness to sign it.
  • Scheduled for a consultation visit with an oncologist to prepare for a radiation therapy for cancer treatment or currently receiving radiation treatment for cancer at a University of California, San Francisco (UCSF) location (Mission Bay, Mount Zion, Parnassus, etc.).
  • Reported using cigarettes, e-cigarette or any tobacco product(s) in the past 12 months

排除标准

  • Contraindication to any study-related procedure or assessment.
  • Participated in Patient/Care Team Advisory Board Activities for the project
  • Hearing and/or vision disabilities in receiving the iMD intervention or follow-up assessment such as videos or telephone interviews at follow-up
  • Cancer care team's judgement of inappropriateness due to cognitive or medical reasons
  • Inability to understand spoken and written English
  • Completion of radiation therapy for cancer at time of enrollment

结局指标

主要结局

Proportion of iMD participants who complete 2 or more sessions

时间窗: Up to 3 months

The proportion of participants enrolled in the iMD arm who complete at least 2 or more of the iMD sessions will be reported.

Proportion of eligible individuals who consent to enroll in the study

时间窗: Up to 6 months

The proportion of participants who consent to enroll from the total number who are approached for eligibility will be reported.

Proportion of participants assigned to iMD intervention with a response to referral question

时间窗: Up to 3 months

The proportion of participants assigned to iMD intervention who have a recorded response to the question on referral to a smoking cessation treatment service/ resource will be reported.

Median scores on the perceived helpfulness of the iMD program

时间窗: Up to 3 months

The perceived helpfulness of the iMD program will be measured using a 5-point likert scale a a response to the question provided to the participants who are assigned to the iMD arm which rates the helpfulness of the intervention as 1='Somewhat helpful" to 5="Very helpful

次要结局

  • Proportion of iMD participants who indicate requests of referral for smoking cessation(Up to 9 months)
  • Proportions of participants with reported abstinence(Up to 3 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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