Examining the Effects of Regular Brief Internet-based Meditation Practice on Mental Health and Well Being
- Conditions
- HealthyWell-Being, Psychological
- Interventions
- Behavioral: SOS Meditation
- Registration Number
- NCT06014281
- Lead Sponsor
- Stanford University
- Brief Summary
The study will examine the effects of online meditation training on stress and anxiety in healthy participants. It will also examine the dose-response relationship between the amount of daily focused attention meditation practice and established mental health outcome measures.
- Detailed Description
This is a 16-week study with an 8-week meditation intervention, with a requirement of a minimum of 10 minutes of meditation practice each day. This study will recruit \~200 healthy subjects (18+ years) with no current or previous diagnosis of psychiatric or neurological disorders who are interested in learning about meditation but don't have long-term experience with meditation. Half of the participant pool will be randomly assigned to the meditation intervention, and the other half will get the wait-list control assignment. The control group will later receive its intervention, likely a few weeks after the completion of the active group's intervention. A focused-attention meditation technique (SOS meditation) will be used to train participants.
Changes in participants' physiological markers (e.g., HRV, physical activity, respiration rate, sleep quality) will be evaluated using passive activity monitoring devices (e.g., Fitbit). Intervention-related changes in mental health will be assessed using web-based mental health and well-being surveys. Improvements in cognitive functioning will be assessed using web-based psychological tasks.
Recruitment & Eligibility
- Status
- ACTIVE_NOT_RECRUITING
- Sex
- All
- Target Recruitment
- 300
- Age ≥ 18 years
- Able to follow basic instructions for prescreening and scheduling
- Compliant with investigator instructions during the consent process and participation in the study
- Is not already a regular meditation practitioner
- Age <18
- People with a current diagnosis of psychiatric or neurological disorders
- Be in current psychiatric treatment or medications
- Hospitalized for psychiatric disorders in the past year or so.
- Regular and long-term meditation practitioners
- Non-English speaking
- Non-USA mailing address to receive the activity tracker device
- Vision or hearing impairment severe enough to interfere with study participation
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Meditation group SOS Meditation Baseline to week 8: Subjects will be trained to meditate for 10 minutes daily, and several measures (questionnaires, cognitive tests, and physiological measurements) will be obtained to assess the efficacy of daily meditation practice on mental health and well being. Focused-attention meditation technique will be used to train participants. Specifically the SOS meditation technique will be employed. Week 8 to week 16: Subjects will self report if they choose to continue SOS meditation and several measures (questionnaires, cognitive tests, and physiological measurements) will be obtained to assess the impact of continued meditation practice on mental health and well being. Waitlist control SOS Meditation Baseline to week 8: Subjects will be place in a control group which receives no intervention. However, several measures (questionnaires, cognitive tests, and physiological measurements) will be obtained to assess baseline mental health and well being scores. Week 8 to week 16: Subjects will be trained to meditate for 10 minutes daily, and several measures (questionnaires, cognitive tests, and physiological measurements) will be obtained to assess the efficacy of daily meditation practice on mental health and well being. Focused-attention meditation technique will be used to train participants. Specifically the SOS meditation technique will be employed.
- Primary Outcome Measures
Name Time Method Change in Stroop Test Score Twice (Baseline and week 8 for arm 1 and week 8 and week 16 for arm 2) Using the Stroop test, which measures the average reaction time between incongruent and congruent trials
Resting Heart Rate Daily (from baseline to week 8 for arm 1 and from week 8 to week 16 for arm 2) Daily obtained from Activity Tracker wrist band
Change in Generalize Anxiety Disorder Questionnaire Score Twice (Baseline and week 8 for arm 1 and week 8 and week 16 for arm 2) Anxiety as measured using Generalize Anxiety Disorder Questionnaire
Change in Pittsburgh Sleep Quality Index Questionnaire Score Twice (Baseline and week 8 for arm 1 and week 8 and week 16 for arm 2) Sleep Quality measured using Pittsburgh sleep quality index (PSQI)
Change in Mind Wandering Questionnaire Score Twice (Baseline and week 8 for arm 1 and week 8 and week 16 for arm 2) Mind wandering measured using the Mind Wandering Questionnaire
Change in N-back Test Score Twice (Baseline and week 8 for arm 1 and week 8 and week 16 for arm 2) Using the N-back test is a memory task where participants must remember letters from N trials ago.
Heart Rate Variability Daily (from baseline to week 8 for arm 1 and from week 8 to week 16 for arm 2) Daily obtained from Activity Tracker wrist band
- Secondary Outcome Measures
Name Time Method Change in Brief Strengths Scale Questionnaire Score Twice (Baseline and week 8 for arm 1 and week 8 and week 16 for arm 2) Strengths scale measured using Brief Strengths Scale measures individuals' Temperance Strength, Intellectual Strength, and Interpersonal Strength.
Change Social Connectedness Scale-Revised Questionnaire Score Twice (Baseline and week 8 for arm 1 and week 8 and week 16 for arm 2) Social Connectedness measured using Social Connectedness Scale-Revised
Change in Depression Questionnaire Score Twice (Baseline and week 8 for arm 1 and week 8 and week 16 for arm 2) Depression measured using Patient Health Questionnaire
Change in Quality of Life Scale Measures Questionnaire Score Twice (Baseline and week 8 for arm 1 and week 8 and week 16 for arm 2) Quality of life measured using Quality of Life Scale measures
Change in Stress Scale Measure Questionnaire Score Twice (Baseline and week 8 for arm 1 and week 8 and week 16 for arm 2) Stress measured using Perceived Stress Scale measure
Change in Rumination Reflection Questionnaire Score Twice (Baseline and week 8 for arm 1 and week 8 and week 16 for arm 2) Rumination and reflection scales measured using Rumination Reflection Questionnaire
Change in Sleep Quality Measure Daily (from baseline to week 8 for arm 1 and from week 8 to week 16 for arm 2) Daily obtained from Activity Tracker wrist band
Trial Locations
- Locations (1)
Dept. of Psychiatry, Stanford University
🇺🇸Stanford, California, United States