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Coping Strategies for Suicidal Thoughts
N/A
Recruiting
Research Sponsored by Massachusetts General Hospital
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up within two hours of each micro-randomization
Awards & highlights
Study Summary
This trial will study if a smartphone intervention can help adults with suicidal thoughts use safety plans & coping strategies and reduce thoughts.
Who is the study for?
This trial is for adults hospitalized with suicidal thoughts who can speak and write English fluently, own a smartphone, and are able to participate fully in the study. Those with cognitive impairments, intellectual disabilities, violent behavior or psychotic symptoms that affect understanding of the study cannot join.Check my eligibility
What is being tested?
The study tests a real-time smartphone-based intervention promoting safety plans and coping strategies to manage suicidal thoughts. It checks if automated reminders increase strategy use and reduce suicidal ideation among participants answering surveys several times daily post-hospitalization.See study design
What are the potential side effects?
Since this trial involves non-medical interventions like coping strategies delivered via smartphones, traditional physical side effects are not expected. However, there may be emotional or psychological responses to the content or process of the intervention.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ within two hours of each micro-randomization
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~within two hours of each micro-randomization
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Extent to which the real-time intervention may be successfully used or implemented as assessed by the Feasibility of Intervention Measure
Intervention engagement as assessed by the number of real-time interventions received and percentage of real-time interventions completed
Participant approval of the real-time intervention as assessed by the Acceptability of Intervention Measure
Secondary outcome measures
Self-reported momentary suicidal urges and intent
Self-reported safety plan and coping strategy use
Trial Design
1Treatment groups
Experimental Treatment
Group I: Real-time intervention for promoting safety plan and coping strategy useExperimental Treatment9 Interventions
Momentary surveys in which elevated (non-zero but < 8 out of 10) levels of suicidal intent or high (>= 8 out of 10) suicidal urges are reported will be randomized either to receive a real-time intervention that consists of automated, interactive reminders with suggested strategies for coping with suicidal thoughts or no intervention.
If randomized to receive an intervention, the intervention type will also be randomized (at equal probabilities) to suggest either coping strategies from the participant's personalized safety plan or general common coping strategies.
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Who is running the clinical trial?
Massachusetts General HospitalLead Sponsor
2,935 Previous Clinical Trials
13,198,616 Total Patients Enrolled
17 Trials studying Suicide
5,128 Patients Enrolled for Suicide
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Eligibility Criteria:
This trial includes the following eligibility criteria:- You are currently having thoughts about hurting yourself while staying in the hospital.
Research Study Groups:
This trial has the following groups:- Group 1: Real-time intervention for promoting safety plan and coping strategy use
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Are there any open vacancies to participate in this medical trial?
"This clinical trial, initially announced on July 5th 2023 and updated lastly on the 6th of that same month, is currently open to patient enrolment according to information available through clinicaltrials.gov."
Answered by AI
How many individuals have opted to participate in this medical inquiry?
"Affirmative. According to the clinicaltrials.gov repository, this trial is actively recruiting participants since its original posting on July 5th 2023 and subsequent update a day later. 25 patients need to be enrolled at two distinct medical sites in order for the study to proceed as planned."
Answered by AI
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