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Examining Feasibility, Acceptability, and Sustainability of a Novel Personalized Smartphone Intervention for Suicide - Open Trial

Butler Hospital logo

Butler Hospital

Status

Completed

Conditions

Suicide, Attempted
Suicidal Ideation
Suicide and Self-harm
Suicide

Treatments

Behavioral: Mobile Application to Prevent Suicide (MAPS)

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT05180383
202012-001
R34MH124971 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

The primary aim of the present study is leverage existing infrastructure to develop novel technological features for a novel personalized smartphone intervention system, called the Mobile Application to Prevent Suicide (MAPS), and to establish feasibility, acceptability, safety, and estimate key parameters for secondary outcomes (i.e., suicidal ideation and behavior; re-hospitalization).

Enrollment

10 patients

Sex

All

Ages

18 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Presence of suicidal ideation and/or suicidal behavior in the past month
  • Between the ages of 18 and 70
  • Able to read, write, and understand English well enough to complete study procedures
  • Owns a smartphone

Exclusion criteria

  • Current psychotic or manic symptoms severe enough to interfere with completion of study procedures

Trial design

Primary purpose

Other

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

10 participants in 1 patient group

Mobile Application to Prevent Suicide (MAPS)
Experimental group
Description:
Participants receiving MAPS will receive the Safety Planning Intervention (SPI) which will be uploaded into the smartphone app. They will be prompted four times per day to complete a brief ecological momentary assessment "check-in" inquiring about their cognitions, affect, and behavior, including suicidal thoughts and behaviors. Based on these responses, they will be provided with coping strategies from their safety plans and from a database of coping strategies created by study staff. They will also have access to emergency phone numbers, the coping strategies database, and can communicate with their study clinician through a text-like interface in the app. They will receive this intervention for one month.
Treatment:
Behavioral: Mobile Application to Prevent Suicide (MAPS)

Trial contacts and locations

2

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Central trial contact

Cheryl Cordeiro

Data sourced from clinicaltrials.gov

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