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Behavioral Intervention

Relational Savoring Intervention for Heart Health

N/A
Recruiting
Led By Jessica L Borelli, PhD
Research Sponsored by University of California, Irvine
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 change from baseline health-related events at 3 months.
Awards & highlights

Study Summary

This trial seeks to reduce cardiometabolic disease risk in underserved Hispanic/Latinx communities by reducing risk for their community service providers. It will use a brief intervention rooted in positive psychology & attachment to promote psychosocial well-being & cardiovascular health. #health

Who is the study for?
This trial is for community service providers working at specific health agencies serving low-income Hispanic/Latinx families. It's designed to help these frontline workers, who are at high risk for heart-related issues due to stress and demographics similar to the communities they serve.Check my eligibility
What is being tested?
The study tests a 'Relational Savoring Intervention' (RS), which aims to improve well-being through positive psychology techniques. The goal is to see if RS can reduce cardiovascular disease risks by improving heart rate variability, sleep quality, exercise habits, diet, job satisfaction, and work effectiveness among participants.See study design
What are the potential side effects?
Since the intervention involves psychological techniques rather than medication or medical procedures, side effects may include emotional discomfort or increased awareness of personal challenges related to work stress and lifestyle habits.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~change from baseline hrv at 3 months.
This trial's timeline: 3 weeks for screening, Varies for treatment, and change from baseline hrv at 3 months. for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Heart rate
Heart rate
Heart rate
+13 more

Trial Design

2Treatment groups
Experimental Treatment
Group I: Waitlist Control GroupExperimental Treatment1 Intervention
In this randomized controlled waitlist design, following a baseline assessment, we will randomly assign CSPs into the experimental group (n = 40) or a waitlist group (n = 40). The experimental group will receive the intervention immediately, whereas the waitlist control will wait 4 weeks and have a second baseline assessment before receiving the intervention. All participants will complete an identical assessment battery at pre-intervention baseline, immediately post-intervention, and 3-months following the intervention.
Group II: Intervention GroupExperimental Treatment1 Intervention
In this randomized controlled waitlist design, following a baseline assessment, we will randomly assign CSPs into the experimental group (n = 40) or a waitlist group (n = 40). The experimental group will receive the intervention immediately, whereas the waitlist control will wait 4 weeks and have a second baseline assessment before receiving the intervention. All participants will complete an identical assessment battery at pre-intervention baseline, immediately post-intervention, and 3-months following the intervention.

Find a Location

Who is running the clinical trial?

University of California, IrvineLead Sponsor
537 Previous Clinical Trials
1,921,560 Total Patients Enrolled
1 Trials studying Heart Rate Variability
40 Patients Enrolled for Heart Rate Variability
National Institute on Minority Health and Health Disparities (NIMHD)NIH
376 Previous Clinical Trials
1,215,076 Total Patients Enrolled
Emory UniversityOTHER
1,632 Previous Clinical Trials
2,556,397 Total Patients Enrolled

Media Library

Relational Savoring Intervention (Behavioral Intervention) Clinical Trial Eligibility Overview. Trial Name: NCT05560893 — N/A
Heart Rate Variability Research Study Groups: Intervention Group, Waitlist Control Group
Heart Rate Variability Clinical Trial 2023: Relational Savoring Intervention Highlights & Side Effects. Trial Name: NCT05560893 — N/A
Relational Savoring Intervention (Behavioral Intervention) 2023 Treatment Timeline for Medical Study. Trial Name: NCT05560893 — N/A

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

How many individuals are being included in this clinical experiment?

"Affirmative. Clinicaltrials.gov records suggest that this medical trial, initially posted on November 2nd 2022, is actively searching for qualified participants. 80 individuals are needed from a single site."

Answered by AI

Are any new participants being sought for this research project?

"Affirmative. According to the clinicaltrials.gov record, this trial is still recruiting participants since its initial posting on November 2nd 2022 and latest update on January 5th 2023. A total of 80 individuals need to be registered from one medical centre."

Answered by AI
~9 spots leftby Jun 2024