Psychometric properties of pain and physical functioning outcome measures in patients with diabetic neuropathic pain.

Not Applicable

• Conditions: Diabetic peripheral neuropathic pain; Neurological - Other neurological disorders; Physical Medicine / Rehabilitation - Physiotherapy; Metabolic and Endocrine - Diabetes

• Registration Number: ACTRN12613000748718
• Lead Sponsor: Professor David G Baxter

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2013-07-04
• Last Update Posted: 13 January 2020

Recruitment & Eligibility

• Status: ot yet recruiting
• Sex: All
• Target Recruitment: 80

Inclusion Criteria

1. Adults with a history of Diabetes; and having symptoms of neuropathic pain for > 3 months and scored 12 or more on Self-complete Leeds Assessment of Neuropathic Symptoms and Signs: (S-LANSS) will be eligible to participate in the study.

2. Participants should be able to understand English and provide informed consent to participate.

Exclusion Criteria

Participants who are unable to comprehend and record outcome measure data will be excluded.

Study & Design

• Study Type: Observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Primary outcome measure-1: Modified Brief Pain Inventory- Diabetic Peripheral Neuropathy Item scale<br><br><br>[Time points: at baseline and at the end of 1st and 3rd month following baseline assessment];Primary outcome measure- 2: Screening of Activity Limitation and Safety Awareness scale<br>[At baseline and at 1 and 3 months after baseline assessment ]

Secondary Outcome Measures

Name	Time	Method
Secondary Outcome measure: The Patient Global Impression of Change scale<br>[At 1 and 3 months after baseline (Primary) assessment]