Recruiting NCT05383157
Brief Mindfulness Intervention for Chronic Pain in Ukraine
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Brief mindfulness, Usual care.
- Who it may be relevant to
- Registry conditions: Chronic Pain. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Ukraine
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Overview
This is a pragmatic randomized controlled trial comparing a single 15-minute mindfulness-based intervention to usual care for patients with chronic pain in Ukraine being seen in a pain clinic.
Interventions
- Behavioral Brief mindfulness
Training in mindfulness focused on breathing and pain sensations to enhance decentering, meta-awareness, and interoceptive awareness. - Other Usual care
Usual pain care as delivered in the clinic involving pain assessment and prescription of analgesics.
Primary outcome measures
- Pain intensity [Time frame: Change from baseline to 20 minutes later.]
Secondary outcome measures (5)
- Pain unpleasantness [Time frame: Change from baseline to 20 minutes later.]
- Positive affect [Time frame: Change from baseline to 20 minutes later.]
- Desire for analgesic medication [Time frame: Change from baseline to 20 minutes later.]
- Anxiety [Time frame: Change from baseline to 20 minutes later.]
- Depression [Time frame: Change from baseline to 20 minutes later.]
Eligibility criteria
Inclusion criteria
- Physician-confirmed chronic pain-related diagnosis
Exclusion criteria
- Cognitive impairment preventing completion of study procedures.
- Other unstable illness judged by medical staff to interfere with study treatment.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Open label
- Primary purpose
- Supportive care
Study locations
Ukraine · 1 center
- Vinnitsa National Medical University — Vinnitsa
Identifiers
NCT: NCT05383157 · 0122U002551