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Sinization of the PBAS Scale and Its Reliability and Validity Testing

Sinization of the PBAS Scale and Its Reliability and Validity Testing

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600122359
Enrollment
Unknown
Registered
2026-04-13
Start date
2026-04-20
Completion date
Unknown
Last updated
2026-04-20

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

Conditions

chronic pain comorbid with insomnia

Interventions

Observation group:NA

Sponsors

Peking University Sixth Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18–80, any gender, with at least a junior high school education; 2. Chronic pain lasting =3 months; 3. Types of pain: various chronic pains (including but not limited to chronic back pain, osteoarthritis, fibromyalgia, neuropathic pain, etc.); 4. Ability to read and understand Chinese, and able to complete questionnaires independently; 5. Voluntarily participate in this study and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Individuals with severe cognitive dysfunction (such as dementia or intellectual disability) (MMSE score = 26) or psychiatric disorders (such as schizophrenia, bipolar disorder in the acute phase) (confirmed by an experienced attending physician through clinical interview) who are unable to cooperate with the questionnaire survey; 2. Individuals with severe systemic diseases of the heart, brain, liver, kidneys, or terminal malignant tumors whose physical condition prevents them from completing the questionnaire; 3. Individuals with severe visual or hearing impairments that affect understanding and completing the questionnaire; those unable to communicate effectively in Chinese; 4. Individuals currently participating in similar studies that may affect the results of this study (such as interventions related to pain or insomnia); 5. Pregnant or breastfeeding women.

Design outcomes

Primary

MeasureTime frame
Cronbach's a coefficient;Item-Level Content Validity Index(I-CVI);Scale-Level Content Validity Index (S-CVI);Factor Loading;Pearson correlation coefficient;Intraclass Correlation Coefficient (ICC);

Countries

China

Contacts

Public ContactYan Shao

Peking University Sixth Hospital

xiangbei1991@bjmu.edu.cn+86 188 1133 2326

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 23, 2026