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Stress-physiology Coherence, Interoception, and Well-being Following Mindfulness Training or Tracking Time Spent on Mobile Device (SCIM)

University of Wisconsin (UW) logo

University of Wisconsin (UW)

Status

Completed

Conditions

Not Seeking to Treat Any Conditions

Treatments

Behavioral: Tracking time spent on mobile device
Behavioral: Mindfulness training

Study type

Interventional

Funder types

Other

Identifiers

NCT04125758
L&S/PSYCHOLOGY/PSYCHOLOGY (Other Identifier)
Protocol Version 6/10/2022 (Other Identifier)
2019-0153
A487400 (Other Identifier)

Details and patient eligibility

About

Chronic stress has been shown to impact long-term emotional and physical health. When nearly three-quarters of Americans report stress at levels that exceed what they consider healthy, there is a desperate need to understand factors that contribute to effective stress regulation. This work seeks to develop a measure tied to awareness and acceptance of stress that has shown promise as a predictor of multiple markers of mental and physical well-being, understand how it relates to awareness of the body, and explore whether it can be trained to alleviate suffering and promote well-being. This study aims to 1) Conceptually replicate and extend previous findings linking greater stress-physiology coherence to higher well-being. 2) Assess whether awareness of physiology is associated with stress-physiology coherence. 3) Explore whether stress-physiology coherence can be trained through a brief mindfulness training intervention.

Enrollment

120 patients

Sex

All

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. Age 18 to 65;
  2. Comfortable reading, writing, and conversing in English
  3. U.S. Citizen or permanent resident (for payment purposes)
  4. Have a smartphone compatible with our study app

Exclusion criteria

  1. Significant past experience with meditation, yoga, tai chi, or qi gong;
  2. Current or past psychotic disorder, Bipolar Disorder, PTSD, or social phobia;
  3. Current, severe major depressive episode;
  4. Current, severe generalized anxiety;
  5. Active prescription stimulant use (current or in the past month);
  6. Active prescription beta-blocker, beta-agonist, anti-high blood pressure, or anti-anxiety medication use (current or in the past month);
  7. Currently pregnant (due to physiological changes);
  8. History of neurological disorder;
  9. Currently diagnosed with high blood pressure, or heart murmur;
  10. Have a pacemaker
  11. Have participated in the Trier Social Stress Test previously

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

120 participants in 2 patient groups

Mindfulness training
Experimental group
Description:
Participants will listen to one to two 3-30 minute audio recordings each day for 4 weeks between study visits (28 days total) through the Healthy Minds @Work smartphone app and record when they listen to each recording on a paper log. The app will also collect data on which recordings, when, and for how long participants listen.
Treatment:
Behavioral: Mindfulness training
Tracking time spent on mobile device
Active Comparator group
Description:
Participants will record how much time they estimate they have spent on their phone in the past 24 hours, each day for 4 weeks (28 days total) between study visits.
Treatment:
Behavioral: Tracking time spent on mobile device

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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