Efficacy of Yoga Based Self-Management Program for Chronic Pain

Chronic Pain Clinical Trial

Official title:

Efficacy of Yoga Based Self-Management Program for Chronic Pain: Community Based Clinical Efficacy Study

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04628130
• Other study ID #: AU0211
• Status: Completed
• Start date: September 17, 2020
• Est. completion date: November 9, 2020

Study information

• Verified date: November 2020
• Source: Aarogyam UK
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

Chronic pain is a major health issue with substantial economic burden.To support chronic pain patients during the COVID-19 pandemic, yoga based self-managed intervention was delivered through tele-health platform. Project was designed as community-based program, creating new social networks for patients, health care providers and academics. Platform to deliver intervention and data collection was AiM COVID mobile app.

Our objective was to determine the efficacy of Yoga based self-management intervention for people living with chronic pain pain intensity, disability and health related quality of life.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 42
• Est. completion date: November 9, 2020
• Est. primary completion date: November 5, 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Chronic pain for at least 3 months

• Having access to internet and video calls

Exclusion Criteria:

• Pregnant or breast-feeding women,

• Patients not willing to give written consent

• Patients with severe psychiatric or personality disorder

• Malignancy

Related Conditions & MeSH terms

• Chronic Pain

Intervention

Other:
• Yoga Therapy
Yoga based self managed practices personalised to chronic pain patients

Locations

Country	Name	City	State
United Kingdom	Patanjali Yog Peeth (UK) Trust	Glasgow	Scotland
United Kingdom	Aarogyam UK	Leicester	Leicestershire

Sponsors (2)

Lead Sponsor	Collaborator
Aarogyam UK	Patanjali Yog Peeth (UK) Trust

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Pain intensity and disability	Pain intensity and related disability was measured through Brief Pain Inventory	From baseline to 6 week post intervention
Primary	Health Related Quality of Life	Quality of life was measured through 36-Item Short-Form Survey	From baseline to 6 week post intervention
Primary	Self-efficacy of pain	Self efficacy was measure through Pain Self-Efficacy Questionnaire	From baseline to 6 week post intervention