- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05350449
Loving Kindness Meditation Among Adults 50 Years and Older
July 3, 2025 updated by: Nirmala Lekhak, PhD, University of Nevada, Las Vegas
The goal of this clinical trial is to test the feasibility and acceptability of loving-kindness meditation among adults 50 years and older.
It will also examine the benefits of this intervention and compare the outcomes between two groups (intervention and wait-list control).
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
The main aim of the research is to assess the feasibility and acceptability of the Loving-kindness meditation intervention among adults 50 years or older.
It will also examine the intervention's preliminary impact on loneliness, self-compassion, cognitive function, and psychological well-being.
The study will use a randomized controlled trial with waitlist control.
Study Type
Interventional
Enrollment (Actual)
59
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Nevada
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Las Vegas, Nevada, United States, 89154
- University of Nevada Las Vegas
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
50 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
• Adults 50 years or older living in Southern Nevada
Exclusion Criteria:
• Cognitive or language barrier that would make it difficult to understand and sign the informed consent
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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No Intervention: Waitlist control
The arm will eventually get the intervention.
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Experimental: Loving kindness meditation
Loving-kindness meditation is a contemplative practice that focuses on developing compassion for oneself and others through mindfulness.
Participants will be shown the recorded loving-kindness training video during the first week of the intervention.
Participants will be encouraged to use the mp3 device with guided meditation recording to practice mindfulness meditation for 20-25 minutes every day for 30 days.
We will also provide participants with a diary to record their daily meditation experiences.
There will be weekly check in.
At 60 days we will do a follow-up data collection.
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Loving-kindness meditation is a type of mindfulness practice where the focus is on love/compassion and kindness for self and others.
The guided meditation will be provided via recording device.
The intervention is 4 week long.
Other Names:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in Loneliness
Time Frame: baseline, immediately post-intervention, and week 4 and week 8 post intervention (follow-up periods).
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A 3-item modified UCLA 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.
We will measure loneliness at baseline, post-intervention and 2 follow-up periods to measure the change in loneliness level because of the loving-kindness meditation intervention.
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baseline, immediately post-intervention, and week 4 and week 8 post intervention (follow-up periods).
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Change in Self-compassion
Time Frame: baseline, immediately post-intervention, and week 4 and week 8 post intervention.
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A 12-item Self-compassion Short form Scale by Kirsten Neff will be used to measure self-compassion.
The scores on this scale rages from 1-5.
The highest scores are indicative of better self-compassion.
We will measure self-compassion at baseline and post-intervention periods to measure the change in self-compassion because of the loving-kindness meditation intervention.
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baseline, immediately post-intervention, and week 4 and week 8 post intervention.
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in Anxiety
Time Frame: baseline, immediately post-intervention, and week 4 and week 8 post intervention.
|
A 4-item PROMIS Emotional Distress: Anxiety Scale will be used to measure anxiety.
The scores on this scale range from 4 to 20, the highest scores indicative of a higher feeling of anxiety.
We will measure anxiety at baseline and post-intervention periods to measure the change in anxiety level because of the loving-kindness meditation intervention.
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baseline, immediately post-intervention, and week 4 and week 8 post intervention.
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Change in Depressive Symptoms
Time Frame: baseline, immediately post-intervention, and week 4 and week 8 post intervention.
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A 10-item Center for Epidemiologic Studies Short Depression Scale will be used to measure depressive symptoms.
The scores on this scale range from 10 to 40, the highest scores indicative of a higher feeling of depression.
We will measure depressive symptoms at baseline and post-intervention periods to measure the change in depressive symptoms because of the loving-kindness meditation intervention.
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baseline, immediately post-intervention, and week 4 and week 8 post intervention.
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Nirmala Lekhak, PhD, University of Nevada, Las Vegas
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
May 2, 2023
Primary Completion (Actual)
October 30, 2023
Study Completion (Actual)
October 30, 2023
Study Registration Dates
First Submitted
April 8, 2022
First Submitted That Met QC Criteria
April 27, 2022
First Posted (Actual)
April 28, 2022
Study Record Updates
Last Update Posted (Actual)
July 4, 2025
Last Update Submitted That Met QC Criteria
July 3, 2025
Last Verified
July 1, 2025
More Information
Terms related to this study
Other Study ID Numbers
- UNLV-2022-148
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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