The Effect of Pain Education Group Therapy and Its Impact on Chronic Pain, Kinesiophobia, and Physical Activity
Physical Activity in Patients With Chronic Pain, Its Adherence to WHO Physical Activity Recommendations, and Its Associations With Kinesiophobia, Central Sensitization, Depression, and Pain Intensity
1 other identifier
interventional
50
1 country
1
Brief Summary
The goal of this clinical trial is to learn if pain knowledge group intervention among chronic pain patients would influence their level of physical activity, pain intensity, depression, kinesiophobia and central sensitization. The main question it aims to answer is: Primary hypothesis: pain education will decrease participants' depression and pain intensity and increase their physical activity. There is no comparison group. Participants will participate in a 6-week pain knowledge intervention where they will be learning about sleep, stress models, physical activity benefits, pain neurobiology, mindfulness, pain medication.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable chronic-pain
Started Apr 2026
Longer than P75 for not_applicable chronic-pain
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
March 13, 2026
CompletedFirst Posted
Study publicly available on registry
March 24, 2026
CompletedStudy Start
First participant enrolled
April 1, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 31, 2030
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 30, 2030
March 30, 2026
March 1, 2026
4.2 years
March 13, 2026
March 24, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Change of pain intensity from baseline to 6-weeks
Pain is measured using Graded Chronic Pain Scale -Revised where the lowest value is 0 and the highest is 100. The higher the score, the more pain the subject feels.
from enrollment to the end of treatment at 6 weeks
Change of pain intensity from baseline to 6-weeks
Pain is measured using Brief Pain Inventory Short form where the lowest value is 0 and the highest value is 10. The higher the score, the more pain the subject feels.
from enrollment to the end of treatment at 6 weeks
Secondary Outcomes (1)
Change in depression from baseline to 6-weeks
from enrollment to the end of treatment at 6 weeks
Study Arms (1)
Pain education intervention
EXPERIMENTALThe participants will receive a 6-week pain education in groups. In addition, they are asked to wear an Actigraph to measure their actual physical activity. The topics in the pain education group are as follows: 1. The pain management team - the patient as the supportive leader of the team 2. Contemporary understanding of the biopsychosocial nature of pain 3. Stress and its impact on pain 4. Use of medications in the treatment of chronic pain 5. Physical activity and its impact on pain 6. Negative thoughts and their impact on pain 7. Use of relaxation and mindfulness techniques in pain management 8. Sleep and sleep hygiene 9. Setbacks and coping with them
Interventions
In one group there will be 8-12 participants who will meet once a week during 6 -weeks time. The educational sessions will be 2-hours long including sometimes some exercises and also reflection of the participants.
Eligibility Criteria
You may qualify if:
- Pain lasting longer than 3 months,
- Consequences resulting from long-term pain (such as decreased physical activity, sleep disturbances, fatigue, low mood, etc.)
You may not qualify if:
- Surgery that occurred less than 3 months prior
- Fracture or limb trauma that occurred less than 3 months prior
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Tartu University Hospital
Tartu, Tartu, 50406, Estonia
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Mati Arendi, PhD
CONTACT
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- SUPPORTIVE CARE
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Lecturer of physiotherapy in the Sports Sciences and Physiotherapy institute
Study Record Dates
First Submitted
March 13, 2026
First Posted
March 24, 2026
Study Start
April 1, 2026
Primary Completion (Estimated)
May 31, 2030
Study Completion (Estimated)
December 30, 2030
Last Updated
March 30, 2026
Record last verified: 2026-03
Data Sharing
- IPD Sharing
- Will not share
We might share the data of the participants on OpenScience Platform