NCT05350449

Brief Summary

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).

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
59

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started May 2023

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

April 8, 2022

Completed
20 days until next milestone

First Posted

Study publicly available on registry

April 28, 2022

Completed
1 year until next milestone

Study Start

First participant enrolled

May 2, 2023

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 30, 2023

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

October 30, 2023

Completed
1.7 years until next milestone

Results Posted

Study results publicly available

July 4, 2025

Completed
Last Updated

July 4, 2025

Status Verified

July 1, 2025

Enrollment Period

6 months

First QC Date

April 8, 2022

Results QC Date

April 2, 2025

Last Update Submit

July 3, 2025

Conditions

Outcome Measures

Primary Outcomes (2)

  • Change in Loneliness

    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.

    baseline, immediately post-intervention, and week 4 and week 8 post intervention (follow-up periods).

  • Change in Self-compassion

    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.

    baseline, immediately post-intervention, and week 4 and week 8 post intervention.

Secondary Outcomes (2)

  • Change in Anxiety

    baseline, immediately post-intervention, and week 4 and week 8 post intervention.

  • Change in Depressive Symptoms

    baseline, immediately post-intervention, and week 4 and week 8 post intervention.

Study Arms (2)

Loving kindness meditation

EXPERIMENTAL

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.

Behavioral: Loving-kindness Meditation

Waitlist control

NO INTERVENTION

The arm will eventually get the intervention.

Interventions

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.

Also known as: mindfulness practice
Loving kindness meditation

Eligibility Criteria

Age50 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Adults 50 years or older living in Southern Nevada

You may not qualify if:

  • Cognitive or language barrier that would make it difficult to understand and sign the informed consent

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Nevada Las Vegas

Las Vegas, Nevada, 89154, United States

Location

Results Point of Contact

Title
Dr. Nirmala Lekhak
Organization
University of Nevada Las Vegas

Study Officials

  • Nirmala Lekhak, PhD

    University of Nevada, Las Vegas

    PRINCIPAL INVESTIGATOR

Publication Agreements

PI is Sponsor Employee
Yes

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant Professor

Study Record Dates

First Submitted

April 8, 2022

First Posted

April 28, 2022

Study Start

May 2, 2023

Primary Completion

October 30, 2023

Study Completion

October 30, 2023

Last Updated

July 4, 2025

Results First Posted

July 4, 2025

Record last verified: 2025-07

Data Sharing

IPD Sharing
Will not share

Locations