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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04313517
Other study ID # AUI01
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 12, 2019
Est. completion date September 21, 2019

Study information

Verified date March 2020
Source Aarogyam UK
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Over the last several decades, occupational stress at workplace comprise a major burden. Office based work are more prone to sedentary lifestyle, postural issues, workplace stress, repetitive strain injury, poor employee health. Workplace wellness programs has been very feasible access to employees at their own convenience and need. Yoga@Work Program was developed to suit the need for information technology workers.


Recruitment information / eligibility

Status Completed
Enrollment 140
Est. completion date September 21, 2019
Est. primary completion date June 18, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria:

- Information Technology employee, or trainee willing and able to participate in a 6-week self-care program during the work day.

- Willing to give informed consent

Exclusion Criteria:

- medical or psychiatric conditions limiting practice of yoga in general

- Cognitive impairment

Study Design


Intervention

Other:
Yoga
Each yoga session included warm-up practices (for the large joints, spine, and extremities), Simple postures (Asana), breathing exercises (pranayama) and meditation/relaxation. All the yoga participants were given handouts to practice everyday at work as its feasible

Locations

Country Name City State
Belgium UNRI Brussels
Hong Kong Ananda Yoga Hong Kong
India NMP Medical Research Institute Jaipur Rajasthan
United Kingdom Yog-Kulam London

Sponsors (5)

Lead Sponsor Collaborator
Aarogyam UK Ananda Yoga (Hong Kong), Brunel University, NMP Medical Research Institute, Vrije Universiteit Brussel

Countries where clinical trial is conducted

Belgium,  Hong Kong,  India,  United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Reductions in occupational stress Perceived Stress Scale From baseline to 6-week post intervention
Secondary Mental health problems General Health questionnaires consists of 12 items, each assessing the severity of a mental problem From baseline to 6-week post intervention
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