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Translation of the Self Completed-Leeds Assessment of Neuropathic Symptoms and Signs Pain Scale

Translation and Validation of the Traditional Chinese-Cantonese Version of the Self Completed-Leeds Assessment of Neuropathic Symptoms and Signs Pain Scale

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02450565
Enrollment
200
Registered
2015-05-21
Start date
2015-07-31
Completion date
2016-06-30
Last updated
2015-05-21

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

Conditions

Chronic Pain, Neuropathic Pain, Nociceptive Pain

Brief summary

Neuropathic pain, described as 'pain arising as a direct consequence of a lesion or disease on the somatosensory system', affects up to 3-9.8% of the investigators' population, but is often underdiagnosed and undertreated. As treatment is different for patients with neuropathic pain and nociceptive pain, it is important to screen for neuropathic pain. Commonly employed questionnaire-based diagnostic tools in English speaking countries include the Leeds Assessment of Neuropathic Symptoms and Signs pain scale (LANSS) and Neuropathic pain questionnaire (NPQ). Self-completed LANSS is particularly useful as it is not restricted to clinician's examination and can be applied in large-scale research. S-LANSS has been successfully translated, validated and used successfully in Arabic and Turkish, but it has not been utilised in the Chinese population. As verbal translations of the English questionnaires used at the bedside may be prone to errors in interpretation and requires medical practitioners to interpret the questions. Therefore a translation and validation study is essential.

Interventions

OTHERQuestionnaire

Sponsors

The University of Hong Kong
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

1. Native Chinese-Cantonese speaker 2. Aged 18 to 80 3. Presence of pain for more than 3 months 4. Able to understand, read and write Traditional Chinese 5. Able to give informed written consent 6. Ability to complete the questionnaire

Exclusion criteria

1. Patients who require active pain treatment and / or intervention within 1 week after the initial consultation 2. Voluntary withdrawal from study at any stage

Design outcomes

Primary

MeasureTime frame
Questionnaire can successfully identify subjects with neuropathic pain, or nociceptive painOne year from commencement of study

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026