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Stress Reduction for Busy Professionals

Pilot Study of a Brief Mind/Body Meditation Intervention for Allina Health Employees

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02194478
Enrollment
101
Registered
2014-07-18
Start date
2013-10-31
Completion date
2014-12-31
Last updated
2016-09-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stress

Keywords

Stress, Meditation, Mind body

Brief summary

This is a pre-post intervention pilot study to evaluate the impact of a 30-minute, 8-week mind-body/meditation intervention on self-reported quality of life in individuals employed by Allina Health. Outcomes will include validated questionnaires for depressive symptomology, perceived stress, anxiety, healthy lifestyle, quality of life as well as biological outcomes of salivary cortisol for a sub-sample of employees.

Interventions

BEHAVIORALMeditation

30 minute, 8 week meditation

Sponsors

Allina Health System
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* Men and women aged 18 to 65 years * Actively-working healthcare professional employed by Allina Health.

Exclusion criteria

* Previous participation in an Allina Health stress reduction program * Non-English speaking

Design outcomes

Primary

MeasureTime frameDescription
Perceived stress change from baseline at week 8Baseline, Week 8Perceived stress will be measured through the Perceived Stress Scale at baseline and week 8.

Secondary

MeasureTime frameDescription
Salivary Cortisol Levels Change from baseline at week 8Baseline, Week 8Salivary samples will be obtained at baseline and week 8.
Lifestyle Profile change from baseline at week 8Baseline, Week 8The Lifestyle Profile questionnaire measures self actualization, health responsibility, exercise, nutrition, interpersonal support, and stress management. It will be administered at baseline and week 8.
Work productivity and activity impairment change from baseline at week 8Baseline, Week 8Work productivity and activity impairment will be measured through the WPAI:GH and will be administered at baseline and week 8.
Promis-29 score change from baseline at week 8Baseline, Week 8The Promis-29 is a 29 item questionnaire measuring physical function, fatigue, pain, depression, anxiety, and social role participation. The questionnaire will be administered at baseline and week 8.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026