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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04580082
Other study ID # 20017 - 01D
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 21, 2020
Est. completion date September 28, 2020

Study information

Verified date October 2020
Source Mazonson & Santas Inc.
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The AMBR Study (ADHOC Mindfulness-Based Research Study) is a randomized controlled trial that examines the effectiveness of teaching mindfulness-based techniques through online lessons to combat loneliness, anxiety, and depression among people living with HIV over the age of 50. It is a substudy of the ADHOC study (ClinicalTrials.gov identifier NCT04311554).


Description:

The AMBR Study is a randomized controlled trial that examines the effectiveness of teaching mindfulness-based techniques through online lessons to combat loneliness, anxiety, and depression among people living with HIV who are over the age of 50 and enrolled in ADHOC (ClinicalTrials.gov identifier NCT04311554). The intervention consists of 14 mindfulness audio lessons, each approximately 20-minutes long. The mindfulness lessons are designed to develop three core skills: concentration (the ability to maintain focus on present-moment experiences), clarity (the ability to pinpoint exactly what you are experiencing in each moment), and equanimity (openness to experience).


Recruitment information / eligibility

Status Completed
Enrollment 202
Est. completion date September 28, 2020
Est. primary completion date September 4, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 50 Years and older
Eligibility Inclusion Criteria:

- ADHOC participant with a score of 4 or higher on the 3-item Loneliness Questionnaire from their ADHOC profile

- Clinical diagnosis of HIV

- Able to read and write in English

- Able and willing to provide online informed consent and complete study activities online

- Access to a smartphone or computer

Exclusion Criteria:

- Acute medical problem(s) requiring immediate inpatient treatment

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Mindfulness lessons
14 lessons on mindfulness, each lasting approximately 20 minutes.

Locations

Country Name City State
United States Mazonson & Santas Inc Larkspur California

Sponsors (1)

Lead Sponsor Collaborator
Mazonson & Santas Inc.

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Loneliness Change in loneliness using the 3-Item Loneliness Questionnaire (3IL). 3IL scores range from 3-9, with higher scores indicating greater loneliness. Baseline and follow-up, 25 days
Secondary Anxiety Change in anxiety using the 7-item Generalized Anxiety scale (GAD-7). GAD-7 scores range from 0-21, with higher scores indicating more anxiety. Baseline and follow-up, 25 days
Secondary Depression Change in depression using the 10-item Center for Epidemiologic Studies Depression scale (CES-D-10). CES-D-10 scores range from 0-30, with higher scores indicating more depression. Baseline and follow-up, 25 days
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