NCT01554501

Brief Summary

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

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
855

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Nov 2007

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

November 1, 2007

Completed
4.3 years until next milestone

First Submitted

Initial submission to the registry

March 1, 2012

Completed
14 days until next milestone

First Posted

Study publicly available on registry

March 15, 2012

Completed
3.7 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2015

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2015

Completed
Last Updated

November 30, 2016

Status Verified

November 1, 2016

Enrollment Period

8.1 years

First QC Date

March 1, 2012

Last Update Submit

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
  • 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.

Sponsors & Collaborators

Study Sites (1)

Yale Stress Center

New Haven, Connecticut, 06519, United States

Location

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

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 1, 2007

Primary Completion

December 1, 2015

Study Completion

December 1, 2015

Last Updated

November 30, 2016

Record last verified: 2016-11

Locations

US(1)