Yoga Therapy for Chronic Tension-Type Headache

March 2, 2019 updated by: NMP Medical Research Institute

Yoga Therapy for Chronic Tension-Type Headache: An Evaluation Study

Chronic tension headache represents a considerable social burden in terms of both costs to the health services and also the costs of lost productivity. Episodic tension-type headache can be treated with rest and analgesics, while chronic tension-type headache demands a more fundamental treatment.

Effectiveness of yoga therapy in the management of chronic tension type headache is limited. In this study, yoga therapy was used to explore its effect on chronic tension-type headache.

Study Overview

Status

Completed

Intervention / Treatment

Study Type

Interventional

Enrollment (Actual)

68

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Rajasthan
      • Jaipur, Rajasthan, India, 302019
        • NMP Medical Research Institue

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 55 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Meeting the diagnostic criteria of CTTH in the international classification of headache disorders, 3rd edition (beta version) (ICHD-III beta);
  • Aged 18-55 years;
  • Having the ability of understanding and completing the headache dairy;
  • Provide written informed consent.

Exclusion Criteria:

  • No headache during the pervious 3 months;
  • Taking any prophylactic medication during the previous one month;
  • Secondary headache or any systematic cause
  • Having serious conditions of the heart, liver, kidney or other organs;
  • In pregnancy or lactation, or planning to be pregnant in 6 months;
  • Drug and Substance abuse
  • Diagnosed psychiatric condition
  • Taking any other complementary and alternative medicines
  • Practicing yoga of any kind in last three months

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Yoga Therapy
Yoga therapy session lasted for 60 minutes consisting physical posture, Breath work, Relaxation, guided meditation, chants and combination techniques for groups sessions.
Yoga therapy is therapeutic application of yoga, specifically designed to treat the condition using physical posture, breathing exercises, guided relaxation and meditation.
Other Names:
  • Yoga

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The number of days with headache
Time Frame: Change from baseline to 12-week of intervention
Number of days with headache every four weeks were assessed through headache diaries
Change from baseline to 12-week of intervention

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The medication intake
Time Frame: Change from baseline to 12 week of intervention
Medication score per month were recorded through headache diaries
Change from baseline to 12 week of intervention
Intensity of Pan
Time Frame: Change from baseline to12 week of intervention
Each headache intensity was measure through 0-10 scale; 0 was no pain and 10 was worst pain
Change from baseline to12 week of intervention
Duration of Pain
Time Frame: Change from baseline to12 week of intervention
Duration of each headache was measured through headache diaries
Change from baseline to12 week of intervention

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Director: PJ John, PhD, Deaprtment of Zoology, University of Rajasthan
  • Study Chair: Chandra M Sharma, DM, SMS Medical College and Hospital

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

April 10, 2010

Primary Completion (Actual)

December 12, 2012

Study Completion (Actual)

January 15, 2013

Study Registration Dates

First Submitted

February 28, 2019

First Submitted That Met QC Criteria

March 2, 2019

First Posted (Actual)

March 5, 2019

Study Record Updates

Last Update Posted (Actual)

March 5, 2019

Last Update Submitted That Met QC Criteria

March 2, 2019

Last Verified

March 1, 2019

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

Undecided

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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