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The Feasibility and Efficacy of an Extremely Brief Mindfulness Practice

The Feasibility and Efficacy of an Extremely Brief Mindfulness Practice

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02953444
Enrollment
42
Registered
2016-11-02
Start date
2016-11-30
Completion date
2018-09-09
Last updated
2018-12-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anxiety, Depression, Mental Disorders

Brief summary

This study will assess the efficacy of brief mindfulness practices on improving mental health in adults who are currently in treatment for mental health concerns. From online instructional videos, each participant will learn a thirty-second or three-minute mindfulness practice that is to be performed at least three times daily over two weeks.

Detailed description

Mindfulness meditation and mindfulness-based therapies have been shown to improve many aspects of psychological functioning in individuals with mental health problems. The purpose of this study is to assess the feasibility, acceptability, and efficacy in improving mental health of brief mindfulness practices in adults currently in treatment for mental health concerns. The entire study will be administered online. From online instructional videos, each participant will learn a thirty-second or three-minute mindfulness practice that is to be performed at least three times daily over two weeks. A delayed-treatment control group will begin the intervention after a two-week waiting period.

Interventions

OTHERThirty-Second Mindfulness Practice
OTHERThree-Minute Mindfulness Practice

Sponsors

Duke University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Regular internet access * Able to listen to audio files * Currently receiving outpatient care * No change in type of psychotherapy during the past month * If taking medications, a stable, unchanging prescription for the previous month * Willingness to sign release of mental health care information * Capacity to provide informed consent

Exclusion criteria

* Does not speak and read English

Design outcomes

Primary

MeasureTime frame
Change in trait mindfulness as measured by the Five Facet Mindfulness Questionnaire (Baer et al. 2006)Baseline, 2 weeks and 4 weeks
Change in perceived stress as measured by the Perceived Stress Scale (Cohen, Kamarck, & Mermelstein, 1983)Baseline, 2 weeks and 4 weeks
Change in anxiety symptoms as measured by the GAD-7, Generalized Anxiety Disorder Scale (Spitzer, Kroenke, Williams, & Löwe, 2006)Baseline, 2 weeks and 4 weeks
Change in mood as measured by the Positive and Negative Affect Schedule (Watson, Clark, & Tellegen, 1988)Baseline, 2 weeks and 4 weeks
Change in quality of life as measured by the Medical Outcomes Study 36-Item Short-Form Health Survey (Ware & Sherbourne, 1992)Baseline, 2 weeks and 4 weeks
Change in depression symptoms as measured by the PHQ-8, Patient Health Questionnaire - depression module (Spitzer, Kroenke, & Williams, 1999)Baseline, 2 weeks and 4 weeks

Secondary

MeasureTime frame
Group difference in intervention's acceptability as measured by qualitative questions1 week into intervention
Change in perspective taking as measured by questions adapted from Hawk, Fischer and Van Kleef, (2011)Baseline, 2 weeks and 4 weeks
Group difference in adherence as measured by frequency of daily brief mindfulness practice useDaily for two weeks of intervention
Group difference in continued brief mindfulness practice use as measured by follow-up questionFollow up (two weeks after intervention)
Change in daily mood measured on a visual analogue scaleDaily for two weeks of intervention
Change in daily stress level measured on a visual analogue scaleDaily for two weeks of intervention
Change in empathy as measured by the Interpersonal Reactivity Index (Davis, 1980) and four questions adapted from Hawk, Fischer and Van Kleef, (2011)Baseline, 2 weeks and 4 weeks

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026