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临床试验/NCT06894849
NCT06894849已完成不适用

Evaluation of a Text Message-Based Approach to Depression Screening Among Cancer Survivors

Medical University of South Carolina1 个研究点 分布在 1 个国家目标入组 79 人开始时间: 2026年1月5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
79
试验地点
1
主要终点
Study Feasibility

研究概览

简要总结

Depression is common among cancer survivors, but current screening methods are not always effective. To help improve depression screening for cancer survivors, this study will conduct a pilot randomized controlled trial (RCT) with 60 participants. The goal is to evaluate whether a text message-based approach to depression screening is feasible, acceptable, and potentially more effective than the current standard of care.

详细描述

This pilot randomized controlled trial aims to evaluate the feasibility, acceptability, and preliminary efficacy of a text message-based depression screening approach for cancer survivors. A total of 60 adult cancer survivors will be enrolled and randomly assigned to either the text message intervention or the usual care depression screening. The intervention involves sending text messages one week before scheduled oncology appointments, inviting participants to complete a depression screening using the PHQ-2, followed by the PHQ-9 for those who screen positive.

The study will assess the feasibility of implementing text message-based screenings, participant acceptability, and compare the efficacy of this method to traditional in-person depression screenings during clinical visits. The primary outcome is feasibility, measured by the proportion of participants completing the screening via text, while secondary outcomes will include acceptability (assessed through participant surveys) and preliminary efficacy (measured by screening completion rates and depression detection).

Eligible participants will be English-speaking cancer survivors aged 18 or older with an upcoming oncology appointment at the Hollings Cancer Center or associated clinics. The study aims to improve current depression screening methods and address challenges such as logistical and system-level barriers in screening cancer survivors for depression.

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 (Investigator)

入排标准

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

入选标准

  • •age > 18 years
  • •diagnosis of cancer
  • •upcoming appointment in an HCC or HCN oncology clinic within 14 days
  • •English proficiency
  • •ownership of a cellphone with SMS text capability.

排除标准

  • 未提供

研究组 & 干预措施

Text-Based Depression Screening

Experimental

干预措施: Text-based depression screening (Behavioral)

Usual Care

Active Comparator

干预措施: Usual care (UC) (Behavioral)

结局指标

主要结局

Study Feasibility

时间窗: 2 weeks after randomization

\>/= 1 response to a text message

次要结局

  • Depression screening(2 weeks)
  • Acceptability(2 weeks)
  • PHQ-2 score(2 weeks)
  • PHQ-9 score(2 weeks)

研究者

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

Evan Graboyes

Professor-Faculty

Medical University of South Carolina

研究点 (1)

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