ClinicalTrials.Veeva

Menu

Study Protocol for a Smartphone Application-based Intervention for Subthreshold Depression

K

Kibi International University

Status

Completed

Conditions

Subthreshold Depression

Treatments

Device: Smartphone Application

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

The investigators plan to conduct a randomized controlled trial to examine whether a Smartphone-based Intervention improves subthreshold depression symptoms compared to no intervention.

The purpose of this pilot randomized controlled trial is to investigate the feasibility of the final randomized controlled trial.

Enrollment

32 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 18 Years and older
  • Males and females
  • Center for Epidemiologic Studies Depression Scale score ≥16
  • Written informed consent prior to participation
  • Owns a smartphone with the iOS® operating system

Exclusion criteria

  • Lifetime history of psychiatric disorders
  • Currently receiving treatment for a mental health problem from a mental health professional
  • Experience of a major depressive episode in the 2 weeks prior to the study, as ascertained using the Mini-International Neuropsychiatric Interview
  • Vision or hearing deficits that negatively impact everyday life

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

32 participants in 2 patient groups

Smartphone Application
Experimental group
Description:
Participants watch a video using the Smartphone Application displaying positive word stimuli.
Treatment:
Device: Smartphone Application
No Intervention
No Intervention group
Description:
No Intervention.

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems