← Back to all trials
Not Yet Recruiting
NCT07828132
Effect of Alexithymia on Treatment Response to Transforaminal Epidural Steroid Injections in Chronic Low Back Pain
Conditions: Chronic Low Back Pain, Radiculopathy, Alexithymia
Sex: All
Ages: 18 Years – N/A
Healthy volunteers: No
Enrollment: 60
Sponsor: Marmara University
Summary
Low back pain and lumbosakral radiculopathy represent common clinical challenges substantially diminishing health-related quality of life and work productivity. Transforaminal Epidural Steroid Injection (TFESI) is widely performed in routine practice to reduce radicular pain, enhance functional capacity, and mitigate the need for surgery. However, clinical response to TFESI remains notably heterogeneous, indicating that biomedical parameters alone may not fully account for treatment efficacy and that psychosocial variables play a critical role.
Alexithymia, defined as difficulty in identifying and describing emotions coupled with an externally oriented cognitive style, is prevalent among individuals with chronic spinal pain and linked to heightened pain perception and affective distress.
This prospective observational cohort study aims to investigate the influence of baseline alexithymia levels (measured by the 20-item Toronto Alexithymia Scale \[TAS-20\]) on treatment response (defined as pain relief and functional improvement) following routine clinically indicated TFESI in patients with chronic low back pain and radiculopathy.
Eligibility Criteria
Inclusion Criteria:
1. Adults aged 18 years or older.
2. Clinical diagnosis of chronic low back pain persisting for at least 3 months.
3. Clinical indication and scheduled for Transforaminal Epidural Steroid Injection (TFESI) due to failure of conservative management.
4. Literate and possessing sufficient cognitive capacity to understand and complete self-report instruments.
5. Voluntary written informed consent.
Exclusion Criteria:
1. Significant cognitive impairment or communication barriers impairing informed consent capacity or questionnaire completion.
2. Active psychotic disorder or current manic episode.
3. Suspected acute self-harm or suicidal risk identified during clinical examination.
4. Chronic back pain secondary to malignancy, acute fracture, or active local/systemic infection.
5. Severe active psychiatric illness currently undergoing medical treatment (e.g., severe mental illness, schizophrenia, bipolar affective disorder).
(Note: Depressive symptoms alone are not an exclusion criterion; they are systematically quantified via HADS and controlled for as covariates).
Source: ClinicalTrials.gov (NCT07828132). StuddyBuddy aggregates publicly available trial information.