NCT01554501

Completed

The Role of Stress in Self-Control, Coping, and Emotion Regu...

Yale University Source

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Other study identifiers

Sponsor study identifier

0710003159

Secondary identifiers

5PL1DA024859-05

NIH

Study Type

observational

Actual enrollment (reported)

855

Locations

1 country

Sites

1

Timeline

Study Start

November 2007

Date type not reported

This date has not been verified as actual or estimated.

Primary Completion

December 2015

Actual (reported)

Study Completion

December 2015

Actual (reported)

Brief Summary

The purpose of this study is to examine the effects of stress on mental and physical health and behavior.

Registry Overview

Registry-reported information. Elapsed time and enrollment totals alone do not measure study progress or recruitment pace.

Recruitment status: completed
Actual enrollment (reported): 855 participants
Study completion date: December 2015
Actual (reported)
Listed locations: 1 countries · 1 sites

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Dates and qualifiers reported by the registry. Estimated dates do not confirm that a milestone has occurred.

Study Start
November 2007
Date type not reported
This date has not been verified as actual or estimated.
First Submitted
March 1, 2012
Actual (reported)
First Posted
March 15, 2012
Actual (reported)
Primary Completion
December 2015
Actual (reported)
Study Completion
December 2015
Actual (reported)

Last Updated: November 30, 2016
Status Verified: November 2016
Last Update Submitted: November 28, 2016

Conditions

Stress

Keywords

stressself-controlemotion regulationhealth

Outcome Measures

Primary Outcomes (1)

Stress response and lifestyle behaviors
Study explores differences in measures of stress as they relate to self-control, coping, emotion regulation and lifestyle and health outcomes.
Baseline

Secondary Outcomes (1)

Biological stress responses
Baseline

Study Arms (1)

Community sample

Eligibility Criteria

Age18 Years - 50 Years

Sexall

Healthy VolunteersYes

Age GroupsAdult (18-64)

Sampling MethodNon-Probability Sample

Study Population

Community sample

You may qualify if:

ages 18-50

Sponsors & Collaborators

National Institute on Drug Abuse (NIDA)
NIHcollaborator
Yale University
Otherlead
National Institutes of Health (NIH)

Study Sites (1)

Yale Stress Center

New Haven, Connecticut, 06519, United States

Biospecimen

Retention: SAMPLES WITH DNA

Blood taken for understanding genetic factors.

MeSH Terms

Conditions

Self-ControlEmotional Regulation

Condition Hierarchy (Ancestors)

Social BehaviorBehavior

Study Officials

Rajita Sinha, PhD
Yale University
PRINCIPAL INVESTIGATOR

Enrollment

855 participants (actual enrollment reported by the registry).

Study Design

Study Type: observational
Observational Model: CASE CONTROL
Time Perspective: PROSPECTIVE
Sponsor Type: OTHER
Responsible Party: PRINCIPAL INVESTIGATOR
PI Title: Professor

Study Record Dates

First Submitted

March 1, 2012

First Posted

March 15, 2012

Study Start

November 2007

Date type not reported

This date has not been verified as actual or estimated.

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able to read and write

You may not qualify if:

Any psychotic disorder or current psychiatric symptoms requiring specific attention, including active symptoms of psychosis or suicidal/homicidal ideation
Pregnant women
Inability to give informed consent
Traumatic brain injury or loss of consciousness

Contact the study team to confirm eligibility.

NIHcollaborator

Primary Completion

December 2015

Actual (reported)

Study Completion

December 2015

Actual (reported)

Last Updated

November 30, 2016

Record last verified: 2016-11

Source record

Download the complete ClinicalTrials.gov record imported by Syfrah, including fields not shown in this page. The registry may contain a newer revision.

Source: ClinicalTrials.gov.

JSON downloads include source attribution and retrieval details alongside the unchanged original record or the separately normalized values.

Registry identifier: NCT01554501
Data provider: ClinicalTrials.gov
Source updated: 2016-11-30
Normalization version: ctgov-legacy-1

Open registry record

Source retrieved: 2026-10-25 22:26:48 UTC

Locations

US(1)

Brief Summary

Registry Overview

Trial Relationships

Related Scientific Literature

Study Timeline

Study Start

First Submitted

First Posted

Primary Completion

Study Completion

Conditions

Keywords

Outcome Measures

Primary Outcomes (1)

Secondary Outcomes (1)

Study Arms (1)

Community sample

Eligibility Criteria

You may qualify if:

Sponsors & Collaborators

Study Sites (1)

Biospecimen

MeSH Terms

Conditions

Condition Hierarchy (Ancestors)

Study Officials

Enrollment

Study Design

Study Record Dates

You may not qualify if:

Source record

Locations