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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04466605
Other study ID # AU/NMP/0921
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 30, 2020
Est. completion date July 6, 2020

Study information

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

Clinical Trial Summary

Covid-19 outbreak and lockdown measures raised significant concerns over clinical management of chronic pain patients around the world. Patients with chronic musculoskeletal pain (CMSP) are at high risk of physical disability, psychological distress, and poor quality of life. Analgesic medications were main management during lockdown, but opioid-related concerns have prompted to find immediate alternatives.

Present study was undertaken to determine whether patients randomized to tele-yoga therapy would experience less pain, disability and improved global health, adherence and satisfaction, compared with patients assigned to usual care.


Recruitment information / eligibility

Status Completed
Enrollment 64
Est. completion date July 6, 2020
Est. primary completion date June 30, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria:

- Patients having pain that was musculoskeletal, defined as regional (joints, limbs, back, neck) or more generalized (fibromyalgia or chronic widespread pain);

- Persistent pain ( =3 months) despite trying conventional treatment.

- Access to virtual platform with internet.

- Ready to give informed consent

Exclusion Criteria:

- Schizophrenia,

- Psychiatric disorder

- Cognitive impairment

- Suicidal ideation

- Current illicit drug use

- Terminal illness

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Tele-yoga therapy
Each session included combinations of different yoga exercises, postures, yoga breathing, yoga relaxation techniques, yoga counselling and meditative practices based on individualisation.
Primary care
Patients will follow standard care provided by primary care physicians including analgesics and self care management.

Locations

Country Name City State
India NMP Medical Research Institute Jaipur Rajasthan

Sponsors (3)

Lead Sponsor Collaborator
Aarogyam UK Dr. Sarvepalli Radhakrishnan Rajasthan Ayurved University, NMP Medical Research Institute

Country where clinical trial is conducted

India, 

Outcome

Type Measure Description Time frame Safety issue
Primary Severity of pain Pain was assessed using the Brief Pain Inventory (BPI), which rates the severity of pain on 4 items (current, worst, least, and average pain in past week) From baseline to 6-week post intervention
Primary Interference of pain Interference of pain in 7 areas (mood, physical activity, work, social activity, relations with others, sleep, enjoyment of life) were reported using BPI From baseline to 6-week post intervention
Secondary Global rating of change in pain 7-point global rating of pain change was used to assess change in pain From baseline to 6-week post interventiona
Secondary Intervention specific satisfaction 10 point scale was used to assess intervention-specific satisfaction From baseline to 6-week post interventiona
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