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NCT Number: NCT06611722

The Differences in the Psychological States of Patients with Different Chronic Hip Pain

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.

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Key information

Age range

16 year–65 year

Sex eligibility

All sexes

Study type

Observational

Primary location

General Hospital of the Chinese People's Liberation Army

Beijing, Beijing Municipality, 100000, China

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Psychological and Functional Assessment

Other

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 outcomes

  1. the Beck Depression Inventory (BDI)

    Time frame: 5 minutes

    The BDI is a self-assessment scale that has been demonstrated to be a reliable and valid tool for evaluating depressive symptoms. The BDI comprises 21 items, each item is assigned a score on a scale of 0 to 3, with higher scores indicating a greater severity of depressive symptoms.

  2. the Zung Self-Rating Anxiety Scale (SAS)

    Time frame: 5 minutes

    The SAS is a self-assessment instrument designed to evaluate the presence and severity of anxiety symptoms. The SAS consists of 20 items, each item consisting of four statements, and each item is scored on a scale of 1 to 4. A higher score indicates a higher level of anxiety.

Secondary outcomes

  1. the Visual Analogue Scale (VAS)

    Time frame: 2 minutes

    for the assessment of the level of hip pain perceived by the patient

  2. the Pain Sensitivity Questionnaire (PSQ)

    Time frame: 5 minutes

    for the assessment of the individual's sensitivity to pain

  3. The Hip Outcome Score Activities of Daily Living (HOS-ADL)

    Time frame: 5 minutes

    evaluate the functional activities necessitated by daily life with the hip

  4. The Hip Outcome Score - Sport-specific subscale (HOS-SSS)

    Time frame: 5 minutes

    assess the capacity to perform sports activities

  5. the modified Harris Hip Score (mHHS)

    Time frame: 5 minutes

    assess the functional level of the hip joint

  6. the international hip outcome tool (IHOT-12)

    Time frame: 5 minutes

    assess the functional level of the hip joint

Sponsors and collaborators

Lead sponsor

ChunBao Li

Other

Registry information

Official study title

A Clinical Retrospective Cross-sectional Study of the Differences in the Psychological States of Patients with Different Chronic Hip Pain

Important dates

Study start
2023
Primary completion
2024
Study completion
2024
First posted
Sep 25, 2024
Registry last updated
Sep 26, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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