Skip to main content
Clinical Trials/NCT06894849
NCT06894849CompletedNot Applicable

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

Medical University of South Carolina1 site in 1 country79 target enrollmentStarted: January 5, 2026Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
79
Locations
1
Primary Endpoint
Study Feasibility

Study Overview

Brief Summary

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.

Detailed Description

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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Supportive Care
Masking
Single (Investigator)

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •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.

Exclusion Criteria

  • Not provided

Arms & Interventions

Text-Based Depression Screening

Experimental

Intervention: Text-based depression screening (Behavioral)

Usual Care

Active Comparator

Intervention: Usual care (UC) (Behavioral)

Outcomes

Primary Outcomes

Study Feasibility

Time Frame: 2 weeks after randomization

\>/= 1 response to a text message

Secondary Outcomes

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

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Evan Graboyes

Professor-Faculty

Medical University of South Carolina

Study Sites (1)

Loading locations...

Similar Trials

Text -Based Depression Screening Among... | Clinical Trial