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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04316455
Other study ID # AU06
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date October 28, 2019
Est. completion date March 7, 2020

Study information

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

Clinical Trial Summary

Chronic pain self-management skills can help patients improve daily functioning and quality of life. The goal of this study is to evaluate chronic pain self-managed Integrative Yoga Therapy intervention delivered in a sample of 25 older adults recruited from community site in Leicester.


Recruitment information / eligibility

Status Completed
Enrollment 25
Est. completion date March 7, 2020
Est. primary completion date February 28, 2020
Accepts healthy volunteers No
Gender All
Age group 60 Years and older
Eligibility Inclusion Criteria:

- Willing to provide informed consent

- Age >= 60 years

- Ambulatory

- Community-living

- Self-reported chronic musculoskeletal pain > 3 months having pain made it difficult to do usual activities

- Ability to attend sessions one in a week for 6-weeks

Exclusion Criteria:

- Serious illness or hospitalisation in last 3-month

- Planned surgery in next six months

- Significant cognitive impairment

- Other severe physical or psychiatric disorder

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Integrative Yoga Therapy
Participants having an hour in-person weekly session with qualified yoga therapist for 6-weeks. At each session, the personalised yoga practices including straightening and relaxing posture of yoga, yoga breathing, Combinations of sound and imagery yoga practices were given and asked to continue practice at home during the week.

Locations

Country Name City State
United Kingdom Karyalaya Leicester Leicestershire

Sponsors (3)

Lead Sponsor Collaborator
Aarogyam UK Hindu Swayamsevak Sangh (UK), Leicester Ageing Together

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Pain severity and interference: Brief Pain Inventory (BPI) questionnaire Pain severity and interference were evaluated by using the Brief Pain Inventory (BPI) questionnaire. From baseline to 6-week post intervention
Secondary Participant Global Impression of Change Participant Global Impression of Change included 2 item the change from baseline From baseline to 6-week post intervention
Secondary Participant satisfaction: Likert-scale questions Likert-scale questions score between 1-5 for participant satisfaction with the program (Strongly Agree=1 to Strongly Disagree=5) From baseline to 6-week post intervention
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