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Illness Perception and Treatment Expectations in Lateral Elbow Pain

Determining the Predictors of Illness Perception and Treatment Expectations in Individuals With Lateral Elbow Pain: A Cross-Sectional Study

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07722845
Acronym
LEP-IPTE
Enrollment
137
Registered
2026-07-23
Start date
2026-07-31
Completion date
2027-01-05
Last updated
2026-07-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Musculoskeletal Pain, Lateral Elbow Pain, Lateral Epicondylitis, Tendinopathy, Tennis Elbow

Keywords

Illness perception, Treatment expectation, Lateral epicondylalgia, Pain catastrophizing, Fear-avoidance beliefs, Pain self-efficacy, Biopsychosocial model, Hierarchical regression

Brief summary

This cross-sectional, correlational study aims to determine the predictors of illness perception and treatment expectations in adults with chronic lateral elbow pain. Sociodemographic characteristics, clinical findings (pain intensity, pain duration, elbow-specific function) and psychosocial variables (pain self-efficacy, fear-avoidance beliefs, pain catastrophizing) will be examined as candidate predictors of two patient-centred constructs: illness perception, measured with the Brief Illness Perception Questionnaire, and treatment expectation, measured with the Treatment Expectation Questionnaire. Data will be analysed using hierarchical multiple linear regression in three predictor blocks. The study is reported according to the STROBE statement.

Interventions

None listed

Sponsors

Acibadem University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Aged 18 years or older * Diagnosis of lateral epicondylalgia or lateral elbow pain made by an orthopaedic surgeon or physiatrist * Pain intensity of at least 4 on the Numeric Rating Scale * Pain duration of at least 12 weeks (chronic) * Willing to provide written informed consent

Exclusion criteria

* History of any surgical procedure of the upper extremity * Cervical spine pathology * Inflammatory arthritis affecting the wrist or finger joints (e.g. rheumatoid arthritis) * Active neurological disease or radiculopathy radiating to the upper extremity * Diagnosis of fibromyalgia or another widespread pain syndrome * Currently receiving active psychiatric treatment (e.g. psychosis, severe depression) * Pregnancy * Visual or cognitive impairment of a degree that would prevent completion of the questionnaires

Design outcomes

Primary

MeasureTime frameDescription
Illness perception (Brief Illness Perception Questionnaire, B-IPQ)Single assessment at enrollment (Day 1)The B-IPQ is a 9-item self-report instrument assessing cognitive and emotional representations of illness. Eight items are rated on a 0 to 10 numeric scale covering consequences, timeline, personal control, treatment control, identity, concern, coherence and emotional representation; the ninth item is open-ended and asks about perceived causes. The total score ranges from 0 to 80, with higher scores indicating a more threatening perception of the illness.
Treatment expectation (Treatment Expectation Questionnaire, TEX-Q)Single assessment at enrollment (Day 1)The TEX-Q assesses expectations of an upcoming treatment. Fifteen scored items are rated on an 11-point scale from 0 (no expectation at all) to 10 (expecting complete recovery from treatment); six additional items are not included in scoring. Higher scores indicate higher treatment expectation.

Secondary

MeasureTime frameDescription
Pain intensity (Numeric Rating Scale, NRS)Single assessment at enrollment (Day 1)Self-reported lateral elbow pain intensity rated from 0 (no pain) to 10 (worst imaginable pain). Higher scores indicate greater pain intensity.
Pain self-efficacy (Pain Self-Efficacy Questionnaire, PSEQ)Single assessment at enrollment (Day 1)Ten items rated on a 7-point Likert scale (0 = not at all confident, 6 = completely confident), giving a total score of 0 to 60. Higher scores indicate greater confidence in performing activities despite pain.
Fear-avoidance beliefs (Fear-Avoidance Beliefs Questionnaire, FABQ)Single assessment at enrollment (Day 1)Sixteen items rated on a 7-point Likert scale from 0 (completely disagree) to 6 (completely agree), assessing beliefs about the effect of physical activity and work on pain. Higher scores indicate stronger fear-avoidance beliefs.
Pain catastrophizing (Pain Catastrophizing Scale, PCS)Single assessment at enrollment (Day 1)Thirteen items with helplessness, magnification and rumination subscales, each rated from 0 (never) to 4 (all the time), giving a total score of 0 to 52. Higher scores indicate greater pain catastrophizing.
Elbow pain and function (Patient-Rated Tennis Elbow Evaluation, PRTEE)Single assessment at enrollment (Day 1)Fifteen items covering pain (5 items) and function (6 specific activity items and 4 usual activity items) over the past week. The total score ranges from 0 to 100, with higher scores indicating greater pain and loss of function.

Countries

Turkey (Türkiye)

Contacts

CONTACTHasan Gercek, PhD
hasan.gercek@acibadem.edu.tr+90 542 648 8455
CONTACTNuray Alaca, PhD
nuray.alaca@acibadem.edu.tr+90 532 425 1290
PRINCIPAL_INVESTIGATORHasan Gercek, PhD

Acibadem University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 24, 2026