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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06075329
Other study ID # UNLV-2023-395
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date December 1, 2023
Est. completion date May 31, 2024

Study information

Verified date October 2023
Source University of Nevada, Las Vegas
Contact Nirmala Lekhak, PhD
Phone 7028955983
Email nirmala.lekhak@unlv.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The goal of this study is to test the contemplative practice is feasible and acceptable among informal dementia caregivers population at all stages.


Description:

It will also examine the benefits of this intervention and compare the outcomes between two groups (intervention and wait-list control).


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 200
Est. completion date May 31, 2024
Est. primary completion date May 31, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Dementia Family Caregivers - At least cared for dementia care receipient more than 6 months Exclusion Criteria: - If they have meditated less than 2 months ago - Cognitive or language barrier that would make it difficult to understand and sign the informed consent

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Contemplative Practice
Contemplative practice included Maitribodh Sambodh Dhyaan (MSD), which was designed to increase feeling of love and connection by including most of components of different contemplative practices such as breath watch, mantra or vibrational sound chant, focused meditation, and visualization followed by loving-kindness or a gratitude exercise at the end.

Locations

Country Name City State
United States University of Nevada Las Vegas Las Vegas Nevada

Sponsors (1)

Lead Sponsor Collaborator
University of Nevada, Las Vegas

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in Loneliness The UCLA 3-item Loneliness scale will be used to measure loneliness. The scores on this scale range from 3 to 9, the highest scores indicative of a higher level of loneliness. The scale is called UCLA 3-item scale but UCLA is representative of University of California Los Angeles. baseline, at 10 days and 21 days of Matribodh Sambodh Dhyaan practice (meditation), and at 30 days and 60 days follow-up.
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