Recruiting

Self-Management Interventions

Sponsor:

University of Washington

Code:

NCT06037785

Conditions

Implantable Defibrillator User

Stress Reaction

Ptsd

Stress Management

Social Cognitive Theory

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Interventions

Self-Paced Self-Management (SPSM)

Study Details

Brief summary:

This study, "Biobehavioral Intervention to Reduce PTSD Symptoms After an ICD Shock," addresses a critical need in cardiology care by describing the feasibility and acceptability of a timely, highly promising, electronically-delivered intervention for patients who have recently received an ICD delivered shock. The study intervention and outcomes are designed to reduce anxiety, enhance return to activities of daily living (ADLs), and prevent the development of severe distress and post-traumatic stress disorder (PTSD), and ultimately promote quality of life. The study is a two-arm, embedded mixed methods, randomized trial (N=60, 30/group). The purpose is to determine feasibility and potential effects of a self-management intervention (SPSM) plus usual care (UC) compared to UC alone, delivered during the critical 1 month period after an ICD shock when distress is high. The intervention will be delivered over 1 month following an ICD shock; a 6-month follow-up will be used to assess the sustainability of intervention effects and determine if the incidence of PTSD is reduced. SPSM includes: 1) training in heart rate (HR) self-monitoring; and 2) individualized learning through 4 self-paced, web-based modules. The study interventions are delivered at a crucial time, closely after an ICD shock when stress is high, but PTSD has not yet developed. The specific aims are to: 1) examine the effects of the SPSM intervention plus UC vs. UC alone on the primary outcome of ICD shock anxiety at 1 and 6 months post-shock event, 2) describe the impact of SPSM plus UC compared to UC alone on the secondary outcomes of total daily physical activity, depression, PTSD symptoms, QOL, salivary cortisol levels, and self-efficacy and outcome expectations at 1 and 6 months post-shock event, and 3) assess feasibility, acceptability, and safety of the SPSM intervention, SDOH will be used to describe differential responses to the SPSM intervention. This study fills a significant gap in the care of patients with an ICD, through the systematic testing of a brief, novel and cost-effective intervention that provides the knowledge and skills to improve quality of life. Study findings will be used to design future larger RCTs to test intervention effectiveness for more diverse samples and settings.

Conditions

Implantable Defibrillator User

Stress Reaction

Ptsd

Stress Management

Social Cognitive Theory

Study ID

NCT06037785

Start date

Oct 1, 2024

Status verified date

Sep, 2025

Completion date

Jul 31, 2026

Anticipated

Primary completion date

Jul 31, 2026

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Inclusion Criteria:

1. ICD implant for primary or secondary prevention of sudden cardiac arrest (SCA),
2. receipt of at least 1 ICD shock, appropriate or inappropriate, one week prior to enrollment;
3. able to read, speak and write English;
4. access to online resources and telephone for study duration.

Exclusion Criteria:

1. current diagnosis of PTSD, schizophrenia or bipolar disorder;
2. Short BLESSED score >6 indicating cognitive dysfunction \[73\];
3. age <18 years;
4. AUDIT-C score ≥4 for alcohol use;
5. regular non-medical use of illicit drugs

Study Design

Enrollment

60 participants

Anticipated

Allocation

Randomized

Intervention Model

Parallel Assignment

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: SPSM intervention

Heart rate self monitoring Online shock management modules

no intervention: usual care

standard observation and post-ICD shock care at each clinic that includes ICD interrogations monitored in-person or via home monitor

Interventions

Self-Paced Self-Management (SPSM)

(SPSM) consists of two components: 1) HR Self-monitoring, and 2) online Shock Management modules (N=4) with weekly telephone coaching, completed over 1 month.

Primary outcome measure

  • ICD Shock anxiety [ Time Frame: Baseline, 1, 6 months ]

Central Contacts and Locations

Central contacts

Cynthia M Dougherty, ARNP, PhD

206 221-7927cindyd@uw.edu

Locations

University of Washington

Recruiting

Seattle, Washington, United States, 98195

Contacts

Cynthia Dougherty, ARNP, PhD

206-221-7927cindyd@u.washington.edu

Principal Investigator:

Cynthia Dougherty, ARNP, PhD

More Information

Sponsor

University of Washington

Last update posted

Sep 24, 2025

Last verified

Sep, 2025

Keywords

  • implantable cardioverter defibrillator
  • ptsd
  • stress management

Trial information was received from ClinicalTrials.gov and was last updated on 2026-10-02. This information was provided to ClinicalTrials.gov by University of Washington on 2025-09-24. Recruitment status is synced daily from ClinicalTrials.gov and may not reflect the sponsor's current status. Confirm during your call.