Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
ID07356635

Investigating Cardiovascular Reactivity and Recovery During Grief Recall With Self-Affirmation as a Potential Intervention

Led by University of South Florida · Updated on 2026-01-21

140

Participants Needed

1

Research Sites

12 weeks

Total Duration

On this page

Sponsors

U

University of South Florida

Lead Sponsor

A

Arizona State University

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are investigating how self-affirmation may affect cardiovascular responses during grief. The study focuses on young adults who have experienced a recent loss, exploring how self-affirmation tasks might influence heart rate, blood pressure, and other cardiovascular measures during and after recalling grief. It also examines the relationship between grief severity and psychological stress including depression, anxiety, and sleep quality. Participants will be randomly assigned to either a self-affirmation task, where they rank personal values and write about their top choice, or a control task involving ranking jellybean flavors. Both tasks last about 10 minutes and are followed by a grief recall interview designed to elicit grief-related stress. Cardiovascular data will be collected throughout, including ECG, impedance cardiography, and blood pressure measurements. The study includes a rest period before tasks and a recovery period afterward. During the visit, participants complete questionnaires on health, grief, depression, anxiety, and stress. Height and weight are measured, and cardiovascular monitoring devices are attached. The study lasts through the self-affirmation/control task, grief recall interview, and a quiet recovery phase. Researchers will analyze cardiovascular reactivity and recovery to grief recall, as well as psychological stress measures. The total involvement includes consent, questionnaires, physiological monitoring, interviews, and final assessments.

CONDITIONS

Brief Title

Cardiovascular Effects of Grieving

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Individuals aged 18 and older who have experienced the death of a family member and/or friend within the last 2 to 18 months.
  • Participants must be fluent in English as all procedures will be conducted in English.
Not Eligible

You will not qualify if you...

  • Individuals with a history of cardiovascular disease or disorders.
  • Individuals who are pregnant.
  • Individuals taking medication that may alter or affect cardiovascular and/or cognitive processes.

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Baseline Assessment and Preparation

Duration - Approximately 1 day

Participants complete questionnaires and have their height and weight measured. Cardiovascular measurement equipment is then attached before resting quietly while physiological data is collected.

1 visit (in-person)

Self-Affirmation or Control Task

Duration - 10 minutes

Participants are randomly assigned to either a self-affirming task or a neutral control task. During this 10-minute task, physiological data is collected to assess cardiovascular responses.

1 visit (in-person)

Grief Recall Interview

Duration - 10 minutes

Participants engage in a guided 10-minute grief recall interview designed to elicit grief and related cardiovascular responses while physiological data is collected.

1 visit (in-person)

Recovery Period

Duration - 10 minutes

Participants sit quietly for a 10-minute recovery period while physiological measurements continue to be collected.

1 visit (in-person)

Post-Intervention Questionnaires

Duration - Approximately 30 minutes

Participants complete additional questionnaires assessing self-worth, grief responses, and psychological states before the study concludes.

1 visit (in-person)

Trial Site Locations

Total: 1 location

1

University of South Florida, Psychology and Communication Sciences and Disorders Lab Building

Tampa, Florida, United States, 33620

Actively Recruiting

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Research Team

K

Kaiyuan Luo, BS, BA

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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Published Research Related To This Trial

The Posttraumatic Stress Disorder Checklist for DSM-5 (PCL-5): Development and Initial Psychometric Evaluation.

Christy A Blevins, Frank W Weathers, Margaret T Davis...

https://pubmed.ncbi.nlm.nih.gov/26606250