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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05262075
Other study ID # 5210387
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 26, 2022
Est. completion date September 5, 2022

Study information

Verified date September 2022
Source Loma Linda University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to explore the experiences and benefits of offering an online mindfulness program that integrates resiliency factors to women.


Description:

The purpose of this study is to explore the experiences and benefits of offering an online mindfulness program that integrates resiliency factors to women. Investigators will recruit participants via email and social media flyers to local community sites as well as approved Loma Linda University affiliated sites. Participants who consent will then complete a Demographic Questionnaire(before initial session of program), Pre and Post Stress Surveys (at the start and end of each session), Five-Facet Mindfulness Questionnaire(before and after completion of the program), and a semi-structured interview after the completion of the program. The program will be done be 20-minutes sessions for 3x/week for 4 weeks.


Recruitment information / eligibility

Status Completed
Enrollment 4
Est. completion date September 5, 2022
Est. primary completion date September 5, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 85 Years
Eligibility Inclusion Criteria: - Women who self-identify as having or who are currently experiencing intimate partner violence - English or Spanish speaking - Between 18 and 85 years old. Exclusion Criteria: - Males - No experience of partner violence - Not fluent in either English or Spanish <18 and >85 years of age

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Online Mindfulness Resiliency Program
An approximate 20 minute online mindfulness resiliency program offered 3/wk x 4 weeks.

Locations

Country Name City State
United States Loma Linda University Loma Linda California

Sponsors (1)

Lead Sponsor Collaborator
Loma Linda University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Level of Stress Participants rate their stress level at the beginning and end of each session on a scale of 1-10. Change between Baseline and Week 5 of mindfulness training
Primary Level of Self-Awareness Self-reported 15-item questionnaire designed to provide information on self-awareness and suggests how effective mindfulness practices are. Responses will be recorded on a Likert scale from 0 to 5. Change between Baseline and Week 5 of mindfulness training
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