Completed

Somatic Psychoeducational Intervention for Emotional and Physical Health

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What is being tested

Somatic Psychoeducational Intervention

Behavioral
Who is being recruted

Trauma and Stressor Related Disorders+10

+ Occupational Stress

+ Burnout, Psychological

From 18 to 89 Years
+2 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Supportive Care Study

Interventional
Study Start: October 2024
See protocol details

Summary

Principal SponsorUniversity of Florida
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: October 15, 2024

Actual date on which the first participant was enrolled.

This study looks at the effects of a program called the Somatic Psychoeducational Intervention on emotional and physical health. It specifically targets how this intervention might help people who have trouble regulating certain bodily systems like those influenced by the hormone oxytocin. The study is important because if the intervention proves beneficial, it could help improve overall functioning and wellness for people dealing with related health issues. Participants in the study are randomly divided into two groups. One group receives the intervention in-person, while the other group participates online. Before starting the program, participants listen to calming music and provide saliva samples to measure changes in oxytocin levels. The intervention involves four classes, and participants are assessed at multiple stages: before, right after, one week later, and one month after the program. These assessments include online questionnaires and saliva samples to evaluate any improvements in health and functioning. Participants are compensated for their time and involvement.

Official TitlePotential Benefits of the Somatic Psychoeducational Intervention for Improving Health and Wellness
NCT06580119
Principal SponsorUniversity of Florida
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

30 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Supportive Care Study

These studies explore ways to improve comfort and daily life for people living with a condition. They may focus on easing symptoms, reducing treatment side effects, or supporting overall well-being.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

From 18 to 89 Years

Range of ages for which participants are eligible to join.

Healthy volunteers allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Trauma and Stressor Related DisordersOccupational StressBurnout, PsychologicalPsychological Well-BeingBehaviorMental DisordersBehavioral SymptomsOccupational DiseasesPersonal SatisfactionStress Disorders, Post-TraumaticStress, PsychologicalWounds and InjuriesStress Disorders, Traumatic

Criteria

1 inclusion criteria required to participate
Individuals are eligible to participate if they are between 18 and 89 years old and are providers at the Jewish Family & Community Services (JFCS)
1 exclusion criteria prevent from participating
Individuals are not eligible to participate if they are under 18 years old or older than 89 years old

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

2 intervention groups are designated in this study

This study does not include a placebo group 

Treatment Groups

Group I

Experimental
Participants will be asked to participate in the 4 intervention classes in person. The pre-intervention and post-intervention assessments will require participants to complete a 20-25-minute online survey via Qualtrics and provide saliva samples.

Group II

Active Comparator
Participants will be asked to participate in the 4 intervention classes virtually. The pre-intervention and post-intervention assessments will require participants to complete a 20-25-minute online survey via Qualtrics and provide saliva samples.

Study Objectives

Primary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Suspended

The LJD Jewish Family & Community Services (JFCS) Headquarters

Jacksonville, United StatesOpen The LJD Jewish Family & Community Services (JFCS) Headquarters in Google Maps
CompletedOne Study Center