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Caring for Vets and Service Members: Caring Contacts for Stressed and Distressed Veterans and Service Members

COVE (Caring for Vets and Service Members)

Status
Active, not recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06136234
Acronym
COVE
Enrollment
521
Registered
2023-11-18
Start date
2024-04-30
Completion date
2026-09-30
Last updated
2025-09-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stress, Distress, Emotional

Keywords

suicidal ideation, suicide cognitions

Brief summary

The goal of this clinical trial is to study stressed or distressed veterans and service members. Researchers will compare Caring Contacts plus best available resources to best available resources alone to see if reduces distress and prevents thoughts of suicide.

Detailed description

The objective of this study is to evaluate whether Caring Contacts via text message are beneficial to veterans and service members experiencing stress or distress. In the past, Caring Contacts interventions have focused on individuals who are already suicidal and not a more general population. In addition, a core objective of this study is to understand the mechanisms of action of Caring Contacts and thus has included an ecological momentary assessment (EMA) component that will allow us to determine when and how Caring Contacts is making an impact. Study aims are to Evaluate if stressed or distressed veterans receiving Caring Contacts are at greater or less risk of suicidal ideation or behavior as evidenced by: Decreased mean and reduction in variability of indicators of suicide risk (motivation to live, passive ideation, active ideation, suicide intent, and urges to harm self) acquired during Ecological Momentary Assessment periods. Reduced risk of suicidal ideation (HASS-I) and cognitions (SCS-R) during follow-up. Examine diverse veterans' experiences with Caring Contacts (i.e., access, satisfaction, preferences, potential mechanisms) Evaluate if veterans receiving Caring Contacts will show a decrease in distress (i.e., isolation, depression, substance use, loneliness, defeat, hopelessness, and psychological pain) Identify potential mechanisms of action for Caring Contacts by exploring the relationship between potential mechanisms (i.e., mattering, connectedness, social responsibility, and entrapment), distress, and suicide risk observed during ecological momentary assessment periods to identify potential mechanisms of action of Caring Contacts on decreasing distress and suicide risk

Interventions

BEHAVIORALCaring Contacts

Caring Contacts are brief, periodic messages sent over 1 year that express unconditional care and concern

BEHAVIORALBest Available Resources Alone

Participants will be offered information about best available resources and will receive an email summarizing the resources with links and contact information. These resources are tailored to best serve the participant based on information they share during the online survey or during conversations with study staff.

Sponsors

Face the Fight
CollaboratorUNKNOWN
University of Washington
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Investigator, Outcomes Assessor)

Masking description

All outcome measures are completed by the participant via online survey.

Intervention model description

Randomized Controlled Trial

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* US service member or veteran * 18 years or older * Lives in the United States * Stressed (recent separation from or in transition out of the military, unemployment, financial strain, unhoused, or suicide loss, etc.) or distressed (isolation, depression, substance use, loneliness, defeat, hopelessness, psychological pain, or suicidal ideation, etc.) * Willingness to be contacted periodically by text message and either email or postal mail

Exclusion criteria

\- Unable to consent due to inability to understand the consent form due to cognitive limitations or insufficient English (as determined by inability to pass the consent quiz items)

Design outcomes

Primary

MeasureTime frameDescription
Suicide CognitionsBaseline and 12 month follow-upSuicide Cognitions Scale - Revised, Min=16, max=80, higher scores indicate more suicidal cognitions.
Suicidal IdeationBaseline and 12 month follow-upHarkavy-Asnis Suicide Scale (HASS-I), adapted version for study procedures. Min=0, max=60, higher scores indicate higher suicidal ideation.
Suicide risk Visual Analog Scales (VAS)3 EMA assessments/day for 14 days at baseline; then either 3 EMA assessments/day for 7 days at 12 months OR 3 EMA assessments/day for 7 days/month for 12 months (depending on EMA condition)Suicide risk indicators rated on Visual Analog Scales (VAS; 0-10) acquired during Ecological Momentary Assessment periods. Core constructs of suicide risk selected and worded to maximize face validity: motivation to live, passive ideation, active ideation, and urges for suicide. Higher scores indicate higher suicidal risk (motivation to live is reverse coded).

Secondary

MeasureTime frameDescription
Substance AbuseBaseline and 12 month follow-upShort Inventory of Problems - Alcohol and Drugs (SIP-AD)
LonelinessBaseline and 12 month follow-upNIH Loneliness Scale, Min=5, max=25, higher scores indicate increased loneliness.
Experience of receiving Caring Contacts12 month follow-upParticipants will be asked to describe their experiences with Caring Contacts via an online survey and a qualitative interview with a subset of participants
DepressionBaseline and 12 month-upPatient Health Questionnaire-9 (PHQ-9), Min=0, max=30, higher scores indicate higher degree of depression severity.
DefeatBaseline and 12 month follow-upThe Defeat Scale, Min=0, max=64, higher scores indicate greater defeat.
HopelessnessBaseline and 12 month follow-upBeck's Hopelessness Scale (BHS), Min=0, max=20, higher scores indicate greater hopelessness.
Psychological PainBaseline and 12 month follow-upUnbearable Psychache Scale-3 (UPS-3), Min=3, max=15, higher scores indicate greater psychological pain.

Other

MeasureTime frameDescription
Potential Mechanism: Personal and Social Responsibility3 EMA assessments/day for 14 days at baseline; then either 3 EMA assessments/day for 7 days at 12 months OR 3 EMA assessments/day for 7 days/month for 12 months (depending on EMA condition)Responsibility Scale acquired during Ecological Momentary Assessment periods. Min=8, max=40, higher scores indicate greater sense personal and social responsibility.
Potential Mechanism: Entrapment3 EMA assessments/day for 14 days at baseline; then either 3 EMA assessments/day for 7 days at 12 months OR 3 EMA assessments/day for 7 days/month for 12 months (depending on EMA condition)A single item, I feel trapped, acquired during Ecological Momentary Assessment periods. Min=1, max=7, higher score indicates increased feelings of entrapment.
Potential Mechanism: Perceived Burdensomeness3 EMA assessments/day for 14 days at baseline; then either 3 EMA assessments/day for 7 days at 12 months OR 3 EMA assessments/day for 7 days/month for 12 months (depending on EMA condition)A single item, I felt that I was a burden to other people, or that they would be better off without me, acquired during Ecological Momentary Assessment periods. Min=1, max=7, higher score indicates increased feelings of burdensomeness.
Potential Mechanism: Mattering3 EMA assessments/day for 14 days at baseline; then either 3 EMA assessments/day for 7 days at 12 months OR 3 EMA assessments/day for 7 days/month for 12 months (depending on EMA condition)General Mattering Scale acquired during Ecological Momentary Assessment periods. Min=5, max=20, higher scores indicate greater sense of mattering.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026