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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05350449
Other study ID # UNLV-2022-148
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 2, 2023
Est. completion date October 30, 2023

Study information

Verified date April 2024
Source University of Nevada, Las Vegas
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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).


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.


Recruitment information / eligibility

Status Completed
Enrollment 59
Est. completion date October 30, 2023
Est. primary completion date October 30, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 50 Years and older
Eligibility 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 Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Loving-kindness Meditation
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.

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 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 range from 5 to 60, the highest scores indicative of better self-compassion. We will measure self-compassion at baseline, mid-intervention, 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.
Primary 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, mid-intervention, and post-intervention periods to measure the change in loneliness level because of the loving-kindness meditation intervention. Change in Loneliness will also be measured by A 3-item Campaign to End Loneliness Measurement Tool. baseline, immediately post-intervention, and week 4 and week 8 post intervention.
Secondary Change in Anxiety 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, mid-intervention, and post-intervention periods to measure the change in anxiety level because of the loving-kindness meditation intervention. baseline, immediately post-intervention, and week 4 and week 8 post intervention.
Secondary Change in Depressive Symptoms 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, mid-intervention, and post-intervention periods to measure the change in depressive symptoms because of the loving-kindness meditation intervention. baseline, immediately post-intervention, and week 4 and week 8 post intervention.
Secondary Change in Cognitive Function A 4-item PROMIS Cognitive Function Scale will be used to measure cognitive function. The scores on this scale range from 4 to 20, the highest scores indicative of a lower level of cognitive function. We will measure cognitive function at baseline, mid-intervention, and post-intervention periods to measure the change in cognitive function because of the loving-kindness meditation intervention. baseline, immediately post-intervention, and week 4 and week 8 post intervention.
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