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Evaluating an Expressive Writing Intervention About Communicatively-Restricted Organizational Stressors

S

Santa Clara University

Status

Completed

Conditions

Stress Disorder

Treatments

Other: Expressive Writing

Study type

Interventional

Funder types

Other

Identifiers

NCT01328665
SCUIRB03282011-1

Details and patient eligibility

About

This project evaluates the effectiveness of an intervention sought to reduce the physical effects of stress related to those issues that individuals cannot successfully communicate with anyone about. To do this, the investigators will be implementing a writing intervention over the course of the 6-week study. The investigators will be asking all participants to complete questionnaires over the course of the study period. The investigators are also asking participants to provide a small blood sample (from a fingerstick procedure) at two times during the study as well as saliva samples during that same time. The primary research question asks if this intervention procedure is effective. The investigators are evaluating total cholesterol, high sensitivity c-reactive protein, and cortisol.

Enrollment

44 patients

Sex

All

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • 110 pounds in weight
  • Ability to fast for 8 hours prior to laboratory visit
  • Staff member at Santa Clara University
  • Certain level of inclusionary pretest stress measure

Exclusion criteria

  • Hepatitis
  • Endocrine Disease
  • Kidney or Liver Disease
  • Cancer (in any form)
  • Cushing's disorder
  • Rheumatological disorders
  • Respiratory Disorders
  • Diabetes
  • High blood pressure
  • Low blood pressure
  • Heart or cardiovascular problems
  • Chemotherapy
  • Current use of alpha or beta blockers, steroids, or hormone replacements
  • Pregnant and/or breastfeeding mothers

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

44 participants in 2 patient groups

Expressive Writing
Experimental group
Description:
Affectionate Writing Intervention for 20 minutes per day, 2 times per week, 6 weeks.
Treatment:
Other: Expressive Writing
No writing
No Intervention group
Description:
Control Group -- No writing

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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