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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03813888
Other study ID # NMP/ Arsha/0092
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 21, 2017
Est. completion date March 12, 2018

Study information

Verified date January 2019
Source NMP Medical Research Institute
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The impact of Arsha Vidya program on cognitive performance was examined in elementary school children. The study compares the effects of arsha vidya after school routine with usual after school routine in healthy 8-11 year-old Indian children.

The main objective of the study is to investigate the effect on cognitive function, behaviour and emotions.


Recruitment information / eligibility

Status Completed
Enrollment 70
Est. completion date March 12, 2018
Est. primary completion date January 15, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 8 Years to 11 Years
Eligibility Inclusion Criteria:

- Be 8 - 11 years of age at the start of the intervention

- Healthy Children

- Not start new activity within the intervention period

- Parental conset

- Parents to allow and participate where needed in intervention

Exclusion Criteria:

- Serious chronic illnesses and diseases

- Diagnosed with any psychiatric illness

- Intake of medication that may affect study outcomes

- not able to continue for 12-weeks of participation

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Arsha Vidya chldren's Group
Yoga, Vedic chants, Vedant sessions, Gita sessions and group activities within the Gurukulam (centre)
Usual Activity group
Usual after school activities at home.

Locations

Country Name City State
India NMP Medical Research Institue Jaipur Rajasthan

Sponsors (3)

Lead Sponsor Collaborator
NMP Medical Research Institute Arsha Vidya Study Centre, Tamilnadu, India, Warwick Research Services

Country where clinical trial is conducted

India, 

Outcome

Type Measure Description Time frame Safety issue
Primary Cognitive function Cognitive functions measured by the Cambridge Neuropsychological Test Automated Battery Change from baseline to 12-week
Secondary Behaviour Behaviour measured by the Behavior Rating Inventory of Executive Function Change from Baseline to 12-weeks
Secondary Attention Attention measured by the D2 Test of Attention Change from baseline to 12-weeks
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