NCT07491549

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

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
50

participants targeted

Target at P25-P50 for not_applicable chronic-pain

Timeline
56mo left

Started Apr 2026

Longer than P75 for not_applicable chronic-pain

Geographic Reach
1 country

1 active site

Status
recruiting

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

Study Progress3%
Apr 2026Dec 2030

First Submitted

Initial submission to the registry

March 13, 2026

Completed
11 days until next milestone

First Posted

Study publicly available on registry

March 24, 2026

Completed
8 days until next milestone

Study Start

First participant enrolled

April 1, 2026

Completed
4.2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 31, 2030

Expected
7 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 30, 2030

Last Updated

March 30, 2026

Status Verified

March 1, 2026

Enrollment Period

4.2 years

First QC Date

March 13, 2026

Last Update Submit

March 24, 2026

Conditions

Keywords

chronic paindepressionpain educationphysical activitykinesiophobia

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

EXPERIMENTAL

The 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

Behavioral: pain education

Interventions

pain educationBEHAVIORAL

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.

Also known as: pain neuroscience education, pain management education
Pain education intervention

Eligibility Criteria

Age16 Years - 65 Years
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

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

RECRUITING

MeSH Terms

Conditions

Chronic PainDepressionMotor ActivityKinesiophobia

Condition Hierarchy (Ancestors)

PainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and SymptomsBehavioral SymptomsBehaviorPhobic DisordersAnxiety DisordersMental Disorders

Central Study Contacts

Hanna Kalajas-Tilga, PhD

CONTACT

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

Locations