Reliability and Cross-cultural Adaptation of the Turkish Version of the Neuropathic Pain Symptom Inventory
1 other identifier
observational
120
1 country
1
Brief Summary
In this study, investigators want to perform the reliability and cross-cultural Adaptation of the Turkish Version of the Neuropathic Pain Symptom Inventory
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Jun 2018
Typical duration for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
May 21, 2018
CompletedFirst Posted
Study publicly available on registry
June 4, 2018
CompletedStudy Start
First participant enrolled
June 10, 2018
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 25, 2020
CompletedStudy Completion
Last participant's last visit for all outcomes
December 30, 2020
CompletedMay 13, 2020
May 1, 2020
2.5 years
May 21, 2018
May 11, 2020
Conditions
Outcome Measures
Primary Outcomes (2)
Reliability and adaptation
Investigators will use linguistic validaiton guideline of Mapi research.
7 weeks
DN4
DN4 has become one of the principal condition-specific outcome measures of neuropathic pain.Investigators will use it for comparing results of NPSI.
5 minutes
Interventions
Investigators will use the Neuropathic Pain Symptom Inventory for assessing neuropathic symptoms
Eligibility Criteria
Patients who have neuropathic symptoms
You may qualify if:
- Age upper 18
- Complaints of neuropathic pain for at least 3 months
You may not qualify if:
- Presence of psychiatric illness
- Cancer pain, unsuccessful lumbar surgeon syndrome etc. mix type pain presence
- Presence of complex regional pain syndrome
- Cognitive impairment (mini-mental test score \<24)
- Native language is not Turkish
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Erenkoy Physical Treatment Nad Rehabilitation Hospital
Istanbul, 34400, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY CHAIR
unsal sarı
ERENKOY PHYSICAL THERAPY AND REHABILITATION HOSPITAL
Study Design
- Study Type
- observational
- Observational Model
- CASE ONLY
- Time Perspective
- PROSPECTIVE
- Target Duration
- 3 Months
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Medical doctor, specialist on physical therapy and rehabilitation
Study Record Dates
First Submitted
May 21, 2018
First Posted
June 4, 2018
Study Start
June 10, 2018
Primary Completion
December 25, 2020
Study Completion
December 30, 2020
Last Updated
May 13, 2020
Record last verified: 2020-05
Data Sharing
- IPD Sharing
- Will not share