The Differences in the Psychological States of Patients with Different Chronic Hip Pain
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: Psychological and Functional Assessment.
- Who it may be relevant to
- Registry conditions: Psychological Disorders, Hip Pain Chronic. Basic parameters: 16 years — 65 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
- China
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
A Clinical Retrospective Cross-sectional Study of the Differences in the Psychological States of Patients with Different Chronic Hip Pain
Overview
Nowadays, studies related to the psychological state of patients with chronic hip pain are still limited, and there is a lack of research on the characteristics of the psychological state of patients with chronic soreness from different pain sources. The goal of this retrospective cross-sectional study was to reveal differences between the psychological states of chronic hip pain patients with different pain sources. The main question it aims to answer is whether there are differences in psychological states among hip pain patients with intra-hip pain, extra-hip pain, and intra-hip combined with extra-hip pain.
Interventions
- Other Psychological and Functional Assessment
Assessment of Pain Sources: Patients are grouped based on intra-articular, extra-articular, or combined intra- and extra-articular hip pain.Psychological Assessment: Depression and anxiety are assessed using standardized questionnaires (e.g., BDI for depression, SAS for anxiety).Functional Assessment: Joint function and pain are evaluated using clinical and patient-reported outcome measures.
Primary outcome measures
- the Beck Depression Inventory (BDI) [Time frame: 5 minutes]
- the Zung Self-Rating Anxiety Scale (SAS) [Time frame: 5 minutes]
Secondary outcome measures (6)
- the Visual Analogue Scale (VAS) [Time frame: 2 minutes]
- the Pain Sensitivity Questionnaire (PSQ) [Time frame: 5 minutes]
- The Hip Outcome Score Activities of Daily Living (HOS-ADL) [Time frame: 5 minutes]
- The Hip Outcome Score - Sport-specific subscale (HOS-SSS) [Time frame: 5 minutes]
- the modified Harris Hip Score (mHHS) [Time frame: 5 minutes]
- the international hip outcome tool (IHOT-12) [Time frame: 5 minutes]
Eligibility criteria
Inclusion criteria
- The subject must be at least 16 years old and of sound mind；
- Chronic hip pain persisting for a duration exceeding 3 months.
Exclusion criteria
- Previous mental illness and cognitive impairment；
- Other serious illnesses such as heart failure, respiratory failure, malignant tumours, severe trauma and other serious illnesses;；
- Chronic pain lasting for more than 3 months in other parts of the body;；
- Use of prescribed opioid drugs exceeding 60 mg morphine equivalent per day or steroid analgesics.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Case-control
Study locations
China · 1 center
- General Hospital of the Chinese People's Liberation Army — Beijing
Identifiers
NCT: NCT06611722 · 2023KY031-KS001