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Efficacy of Yoga Based Self-Management Program for Chronic Pain

Sponsor
Aarogyam UK (Other)
Overall Status
Completed
CT.gov ID
NCT04628130
Collaborator
Patanjali Yog Peeth (UK) Trust (Other)
42
Enrollment
2
Locations
1.7
Actual Duration (Months)
21
Patients Per Site
12.1
Patients Per Site Per Month

Study Details

Study Description

Brief 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.

Condition or Disease Intervention/Treatment Phase
  • Other: Yoga Therapy

Study Design

Study Type:
Observational
Actual Enrollment :
42 participants
Observational Model:
Ecologic or Community
Time Perspective:
Retrospective
Official Title:
Efficacy of Yoga Based Self-Management Program for Chronic Pain: Community Based Clinical Efficacy Study
Actual Study Start Date :
Sep 17, 2020
Actual Primary Completion Date :
Nov 5, 2020
Actual Study Completion Date :
Nov 9, 2020

Outcome Measures

Primary Outcome Measures

  1. Pain intensity and disability [From baseline to 6 week post intervention]

    Pain intensity and related disability was measured through Brief Pain Inventory

  2. Health Related Quality of Life [From baseline to 6 week post intervention]

    Quality of life was measured through 36-Item Short-Form Survey

  3. Self-efficacy of pain [From baseline to 6 week post intervention]

    Self efficacy was measure through Pain Self-Efficacy Questionnaire

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Aarogyam UK Leicester Leicestershire United Kingdom
2 Patanjali Yog Peeth (UK) Trust Glasgow Scotland United Kingdom

Sponsors and Collaborators

  • Aarogyam UK
  • Patanjali Yog Peeth (UK) Trust

Investigators

  • Principal Investigator: Neha Sharma, Aarogyam UK
  • Study Chair: Deepa Modi, East Park Medical Centre, NHS trust, Leicester
  • Study Director: Vishwesh Kulkarni, University of Warwick
  • Principal Investigator: Sunita Poddar, Patanjali Yog Peeth (UK) Trust

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Aarogyam UK
ClinicalTrials.gov Identifier:
NCT04628130
Other Study ID Numbers:
  • AU0211
First Posted:
Nov 13, 2020
Last Update Posted:
Nov 13, 2020
Last Verified:
Nov 1, 2020
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:
Chronic Pain

Study Results

No Results Posted as of Nov 13, 2020