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NCT Number: NCT06037785

Self-Management Interventions After an ICD Shock

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Washington

Seattle, Washington, 98195, United States

Location status: Recruiting

Location contact

Cynthia Dougherty, ARNP, PhD

CONTACT

[email protected]

206-221-7927

Cynthia Dougherty, ARNP, PhD

PRINCIPAL_INVESTIGATOR

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

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

Exclusion criteria

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

Treatment and study plan

Self-Paced Self-Management (SPSM)

Behavioral

(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 outcomes

  1. ICD Shock anxiety

    Time frame: Baseline, 1, 6 months

    Florida Shock Anxiety Scale: range 1-50, higher is higher anxiety.

Secondary outcomes

  1. Total daily physical activity(steps/day)

    Time frame: Baseline, 1, 6 months

    Step Watch Activity Monitor, 0-unlimited number of steps. Higher is more steps.

  2. Depression

    Time frame: Baseline, 1, 6 months

    PHQ-9, 0-27. Higher is higher depression.

  3. PTSD Symptoms

    Time frame: Baseline, 1, 6 months

    Post-traumatic Stress Disorder Checklist PCL-5, 0-80. Higher is higher PTSD symtpoms

  4. Quality of Life-Physical and Mental

    Time frame: Baseline, 1, 6 months

    PROMIS Global v 2.0, 0-50. Higher is higher qol.

  5. Self-Efficacy Expectations

    Time frame: Baseline, 1, 6 months

    Self-Efficacy Expectations-SE scale, 0-60, Higher is more self-efficacy

  6. Outcome expectation, 0-90. Higher is higher OE.

    Time frame: Baseline, 1, 6 months

    OE Scale

  7. Salivary cortisol

    Time frame: Baseline, 1, 6 months

    Cortisol in saliva, the range in humans varies. measured in pg/ml.

  8. Acceptability

    Time frame: 6 months

    Acceptability of interventions and materials measured in terms of patient burden (time to complete questionnaires & data collection, ease in understanding, implementing the intervention). These are qualitative open ended answers to questions and do not produce a number.

Other outcomes

  1. Feasibility of implementing the intervention (composite outcome)

    Time frame: 6 months

    Feasibility will be measured using patient recruitment and contact rates (reach within 1-3 days of shock, number screened, eligible & enrolled, proportion eligible vs agree to participate). Each of these variables creates a number for the total study. They elements are added together to get a score.

  2. Safety (composite outcome) of the intervention

    Time frame: 2 years of the trial

    Safety: major adverse cardiac events, including mortality (all cause and cardiac). This is measured as yes or no. Each outcome is score and the total number is summarized.

  3. Acceptability of the intervention (composite outcome)

    Time frame: 6 months

    Acceptability of interventions and materials measured in terms of patient burden (time to complete questionnaires & data collection, ease in understanding, implementing the intervention). These are qualitative open ended answers to questions and do not produce a number.

Study contacts

Contact information is provided by the study sponsor or research team.

Cynthia M Dougherty, ARNP, PhD

CONTACT

[email protected]

206 221-7927

Sponsors and collaborators

Lead sponsor

University of Washington

Other

Collaborators

  • East Carolina University
  • National Institute of Nursing Research (NINR)

Registry information

Official study title

Biobehavioral Intervention to Reduce PTSD After ICD Shock

Important dates

Study start
2024
Primary completion
2026
Study completion
2026
First posted
Sep 14, 2023
Registry last updated
Sep 24, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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