← Eichor
Study identifier: NCT07491549 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

The Effect of Pain Education Group Therapy and Its Impact on Chronic Pain, Kinesiophobia, and Physical Activity

Condition: Chronic Pain  ·  Sponsor: University of Tartu

PhaseNA
Planned participants50
Who can joinAll sexes, 16 Years to 65 Years
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Hanna Kalajas-Tilga, PhD  ·  +372 5816 1041  ·  hanna.kalajas-tilga@ut.ee

Mati Arendi, PhD

Always discuss trial participation with your own doctor first.

Locations (1)

Tartu University HospitalTartu, Tartu, EstoniaRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT07491549