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Integrative Yoga Therapy for Patients With Chronic Pain and Psychological Distress

Integrative Yoga Therapy for Patients With Chronic Pain and Psychological Distress

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04315805
Enrollment
72
Registered
2020-03-20
Start date
2020-06-15
Completion date
2020-12-15
Last updated
2020-03-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Pain, Psychological Distress

Brief summary

This study will be a randomized wait list controlled trial studying the efficacy of an Integrative Yoga Therapy for patients with chronic pain and psychological distress. Individualised yoga program will consist of a 8-week guided self-help program. This study will primarily investigate whether an individually tailored yoga can be beneficial for patients suffering from chronic pain reducing pain, anxiety depression, while improving overall quality of life.

Interventions

Yoga therapy will be based on personalised care consisting of Yoga relaxing posture, strengthening exercise, Yoga breathing, meditative psychotherapy, sound and imagery yoga practices, relaxation, yoga diet and life style management.

Sponsors

Aarogyam UK
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Experienced pain for \> 3 months * Experiences at least one type of psychological distress such as: depression, anxiety, insomnia or stress * Willing to provide informed consent

Exclusion criteria

* Severe medical or psychiatric conditions * Alcohol or substance abuse * Active suicidality * Terminal illness

Design outcomes

Primary

MeasureTime frameDescription
Pain Severity: Visual Analogue ScaleFrom baseline to 8-week post interventionVisual Analogue Scale ranging between 0-10 where 0 is no pain at all and 10 is worst pain
Pain DisabilityFrom baseline to 8-week post interventionChange in pain disability using Pain Disability Index (PDI) with 7 item.Each item scores on 0-10 numeric rating scale in which 0 means no disability and 10 is maximum disability
Symptoms of depression and anxietyFrom baseline to 8-week post interventionHospital Anxiety Depression Scale with 14 item. Each item on the questionnaire is scored from 0-3 where higher score represents increased anxiety and depression levels

Secondary

MeasureTime frameDescription
Insomnia symptomsFrom baseline to 8-week post interventionInsomnia Severity Index has seven questions each scores between 0-4. Higher score defines severity of clinical insomnia
Mental well-beingFrom baseline to 8-week post interventionThe Short Warwick-Edinburgh Mental Wellbeing Scale; Minimum score: 7; maximum score: 35; higher score indicates greater level of wellbeing
Self Efficacy: Pain Self-Efficacy Questionnaire (PSEQ)- 2 item scaleFrom baseline to 8-week post interventionPain Self-Efficacy Questionnaire (PSEQ)- 2 item scale

Countries

United Kingdom

Contacts

Primary ContactUsha Solanki
ukaarogyam@gmail.com+447448307225

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026