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Brief Trainings to Buffer Against Acute Stress Effects

Brief Trainings to Buffer Against Acute Stress Effects

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02214264
Enrollment
172
Registered
2014-08-12
Start date
2014-10-31
Completion date
2015-05-31
Last updated
2019-05-23

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

Conditions

Stress

Brief summary

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.

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.

Interventions

BEHAVIORALLoving-Kindness meditation training

Participants undergo training for approximately 12 minutes. Training involves guided reflections and intentions related to feeling loving-kindness towards the self and others.

BEHAVIORALBreath Awareness meditation training

Participants undergo training for approximately 12 minutes. Training involves guided awareness focused on sensations of breathing.

BEHAVIORALGratitude

Participants undergo training for approximately 12 minutes. Training involves reflections of gratitude for people, events, and things in one's life.

BEHAVIORALControl

Participants will write and then think about the physical space in which they live (i.e., their home) for approximately 12 minutes.

Sponsors

University of Wisconsin, Madison
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

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

Inclusion criteria

* undergraduate psychology recruitment pool

Exclusion criteria

* non-native English speakers, pregnant women

Design outcomes

Primary

MeasureTime frame
Implicit Positive and Negative Affect Test after post-test1 minute after post-test
Change from baseline performance on Operational Span taskBaseline and 10 minutes following post stress induction
Change from baseline in time spent on hand grip self regulation taskBaseline and 30 minutes post stress induction
Change from baseline on likeability ratings of neutral stimuliBaseline and 1 minute post stress induction
Number of trials completed in optional Generosity task40 minutes post stress induction
Positive and Negative Affect Schedule ratings at baselineBaseline
Positive and Negative Affect Schedule ratings after pre-test measures2 minutes before training
Positive and Negative Affect Schedule ratings after training1 minute after training
Positive and Negative Affect Schedule ratings after stress induction1 minute after stress induction
Positive and Negative Affect Schedule ratings after post-test1 minute after post-test measures
Implicit Positive and Negative Affect Test at baselineBaseline
Implicit Positive and Negative Affect Test after pre-test measures2 minutes before training
Implicit Positive and Negative Affect Test after training1 minute after training
Implicit Positive and Negative Affect Test after stress induction1 minute after stress induction

Secondary

MeasureTime frameDescription
Participant interest in participating in future training40 minutes post stress inductionInterest will be rated using a visual analog scale.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 16, 2026