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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02852174
Other study ID # 16648
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 2016
Est. completion date November 2017

Study information

Verified date April 2018
Source University of Illinois at Urbana-Champaign
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Caring for a disabled adult, particularly those with long-lasting impairment, has been associated with elevated levels of stress, depression and anxiety among caregivers.Recent studies show that veteran caregivers experience higher levels of psychological distress than caregivers in the general population, highlighting the psychological needs of this population. The Veteran Caregiver Reducing Stress Time (VetCareReST) is a randomized control trial designed to test the effectiveness of a mindfulness at reducing stress, depression and anxiety in veteran caregivers in Champaign and Danville County.


Description:

Recent estimates indicate that there are 275,000 to one million informal veteran caregivers. Caring for a disabled adult, particularly those with long-lasting impairment, has been associated with elevated levels of stress, depression and anxiety among caregivers. Veteran caregivers are especially vulnerable because of competing demands. For instance, Post 9/11 veteran caregivers are more likely to be the spouse of a veteran, and have experienced the stress of multiple deployments, have a young child in their care, and work outside the home. Recent studies show that veteran caregivers experience higher levels of psychological distress than caregivers in the general population, highlighting the psychological needs of this population. One effective approach at reducing stress, depression and anxiety has been the use of mindfulness training, which has been shown to effectively reduce mood symptoms among professional caregivers. The Veteran Caregiver Reducing Stress Time (VetCareReST) is a randomized control trial designed to test the effectiveness of a mindfulness at reducing stress, depression and anxiety in veteran caregivers in Champaign and Danville County. This study builds on Dr. Lara-Cinisomo's (PI) experience with military spouses. The findings from this trial will serve as pilot data for a large-scale study.


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date November 2017
Est. primary completion date November 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Provide unpaid caregiver or support to a veteran

- Must be 18 years of age or older

- Willing to participate for the duration of the project

- Able to track his/her home practice in a handwritten log

- Have no significant psychiatric disorders other than depression or anxiety (e.g., bipolar disorder, substance abuse, actively suicidal)

Exclusion Criteria:

- The presence of significant psychiatric disorders other than depression or anxiety (e.g., bipolar disorder, substance abuse, actively suicidal)

Study Design


Related Conditions & MeSH terms

  • Stress, Depression, Anxiety and Worry

Intervention

Behavioral:
Mindfulness meditation training
Mindfulness meditation training

Locations

Country Name City State
United States University of Illinois at Urbana-Champaign Champaign Illinois

Sponsors (1)

Lead Sponsor Collaborator
Sandraluz Lara-Cinisomo

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Other Anxiety Anxious symptoms 8 weeks
Other Worry Worried feelings 8 weeks
Primary Stress Perceived levels of stress 8 weeks
Secondary Depressed mood Depressive symptoms 8 weeks