Brief Trainings to Buffer Against Acute Stress Effects

May 21, 2019 updated by: University of Wisconsin, Madison
The purpose of this study is to evaluate and compare the effectiveness of several brief trainings based on contemplative practices and positive psychology to buffer against the negative effects that acute stress has on behavior and cognitive abilities. The investigators hypothesize that training will buffer against negative effects of acute stress.

Study Overview

Detailed Description

Participants will be taught a stress reducing training (breath awareness, loving kindness practice, gratitude exercise) and will practice using this technique for 10-15 minutes. Following this, all participants will undergo the Cold Pressor Task (CPT) for up to 3 minutes.

Before and after these tasks, participant data related to attention, working memory, self regulation, affect, and prosociality will be collected.

Study Type

Interventional

Enrollment (Actual)

172

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Wisconsin
      • Madison, Wisconsin, United States, 53705
        • University of Wisconsin-Madison

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • undergraduate psychology recruitment pool

Exclusion Criteria:

  • non-native English speakers, pregnant women

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Basic Science
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Loving-Kindness training
Participants receive Loving-Kindness meditation training for approximately 12 minutes.
Participants undergo training for approximately 12 minutes. Training involves guided reflections and intentions related to feeling loving-kindness towards the self and others.
Experimental: Breath Awareness training
Participants receive Breath Awareness meditation training for approximately 12 minutes.
Participants undergo training for approximately 12 minutes. Training involves guided awareness focused on sensations of breathing.
Experimental: Gratitude training
Participants will receive Gratitude training for approximately 12 minutes.
Participants undergo training for approximately 12 minutes. Training involves reflections of gratitude for people, events, and things in one's life.
Other: Control
Participants write and then think about the physical space in which they live (i.e., their home) for approximately 12 minutes.
Participants will write and then think about the physical space in which they live (i.e., their home) for approximately 12 minutes.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Change from baseline performance on Operational Span task
Time Frame: Baseline and 10 minutes following post stress induction
Baseline and 10 minutes following post stress induction
Change from baseline in time spent on hand grip self regulation task
Time Frame: Baseline and 30 minutes post stress induction
Baseline and 30 minutes post stress induction
Change from baseline on likeability ratings of neutral stimuli
Time Frame: Baseline and 1 minute post stress induction
Baseline and 1 minute post stress induction
Number of trials completed in optional Generosity task
Time Frame: 40 minutes post stress induction
40 minutes post stress induction
Positive and Negative Affect Schedule ratings at baseline
Time Frame: Baseline
Baseline
Positive and Negative Affect Schedule ratings after pre-test measures
Time Frame: 2 minutes before training
2 minutes before training
Positive and Negative Affect Schedule ratings after training
Time Frame: 1 minute after training
1 minute after training
Positive and Negative Affect Schedule ratings after stress induction
Time Frame: 1 minute after stress induction
1 minute after stress induction
Positive and Negative Affect Schedule ratings after post-test
Time Frame: 1 minute after post-test measures
1 minute after post-test measures
Implicit Positive and Negative Affect Test at baseline
Time Frame: Baseline
Baseline
Implicit Positive and Negative Affect Test after pre-test measures
Time Frame: 2 minutes before training
2 minutes before training
Implicit Positive and Negative Affect Test after training
Time Frame: 1 minute after training
1 minute after training
Implicit Positive and Negative Affect Test after stress induction
Time Frame: 1 minute after stress induction
1 minute after stress induction
Implicit Positive and Negative Affect Test after post-test
Time Frame: 1 minute after post-test
1 minute after post-test

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Participant interest in participating in future training
Time Frame: 40 minutes post stress induction
Interest will be rated using a visual analog scale.
40 minutes post stress induction

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Stacey Schaefer, University of Wisconsin, Madison

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

October 1, 2014

Primary Completion (Actual)

May 1, 2015

Study Completion (Actual)

May 1, 2015

Study Registration Dates

First Submitted

July 31, 2014

First Submitted That Met QC Criteria

August 7, 2014

First Posted (Estimate)

August 12, 2014

Study Record Updates

Last Update Posted (Actual)

May 23, 2019

Last Update Submitted That Met QC Criteria

May 21, 2019

Last Verified

May 1, 2019

More Information

Terms related to this study

Other Study ID Numbers

  • 2014-0572
  • MLK2014 (Other Identifier: Study Team)

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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