Comparison of Stress Reduction Techniques

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

100 participants

Study Classification

INTERVENTIONAL

Study Start Date

2015-04-30

Study Completion Date

2016-08-31

Brief Summary

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There are many ways to reduce stress. This study will compare 2 different programs for reducing stress. In addition to looking at how well the programs reduce stress, we will also ask questions about how these programs may be working.

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Detailed Description

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Conditions

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Stress

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Participants Outcome Assessors

Study Groups

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Program 1

Group Type ACTIVE_COMPARATOR

Program 1

Intervention Type BEHAVIORAL

A well-established behavioral method for reducing stress. To maintain blinding, details will be given to participants after randomization.

Program 2

Group Type ACTIVE_COMPARATOR

Program 2

Intervention Type BEHAVIORAL

A well-established behavioral method for reducing stress. To maintain blinding, details will be given to participants after randomization.

Interventions

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Program 2

A well-established behavioral method for reducing stress. To maintain blinding, details will be given to participants after randomization.

Intervention Type BEHAVIORAL

Program 1

A well-established behavioral method for reducing stress. To maintain blinding, details will be given to participants after randomization.

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* 25-50 years of age
* Able to engage in moderate physical activity
* Interested in being treated for stress

Exclusion Criteria

* Use of psychotropic medications within 6 months prior to study.
* History of extreme physical or psychological trauma.
* Medical conditions that would interfere with study procedures or confound results, such as diabetes, pregnancy, or paralysis.
* Axis I psychiatric diagnosis; e.g., history of substance use disorder, psychotic disorder, bipolar disorder, or eating disorder.

Minimum Eligible Age

25 Years

Maximum Eligible Age

50 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes