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Clinical Trials/NCT03965884
NCT03965884
Completed
Not Applicable

Investigation of the Effects of Lumbal Stabilization Exercises and Connective Tissue Massage on Neuropathic Pain, Functional Capacity and Quality of Life in Patients With Peripheral Neuropathy

Hacettepe University1 site in 1 country8 target enrollmentApril 18, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Peripheral Neuropathy
Sponsor
Hacettepe University
Enrollment
8
Locations
1
Primary Endpoint
Visual Analog Scale
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

The aim of the study is to investigate the efficacy of connective tissue massage and lumbar stabilization exercise treatment on pain severity, functional capacity and quality of life in those who have experienced peripheral neuropathy

Detailed Description

The patients diagnosed with fine fiber neuropathy by the neurology department of hacettepe university will be included and the patients referred to physical therapy will be included. Patients meeting the inclusion criteria will be randomly divided into 3 groups by simple randomization. The first group consisted of lumbal stabilization exercises, the second group with connective tissue massage and the third group with only medical treatment. All patients will be evaluated 2 times before and after 6 weeks. The treatment will be 2 days per week for 6 weeks. Exercise programs of the patients will be performed under the supervision of physiotherapist. In the first group, lumbal stabilization exercises will be applied for 6 weeks and the second group will be given connective tissue massage. Statistical analysis of the study will be done using SPSS 21 statistical program. In the statistical analysis to be carried out within the scope of the study, p value will be selected as 0.05 and p \<0.05 will be considered significant. Mean ± standard deviation, number, percentage, minimum and maximum values will be used as descriptive statistics. Wilcoxon test is used to compare the pre- and post-treatment values of the groups in the variables and the Kruskal-Wallis test will be used to compare the groups with each other.

Registry
clinicaltrials.gov
Start Date
April 18, 2018
End Date
June 15, 2019
Last Updated
6 years ago
Study Type
Interventional
Study Design
Factorial
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

burcu şahin

physiotherapist

Hacettepe University

Eligibility Criteria

Inclusion Criteria

  • diagnosed small fiber neuropathy
  • Score-4 and over from the -DN4 score
  • 18-65 years old adults
  • Volunteers to participate in the study.

Exclusion Criteria

  • Pain from different etiologies
  • Other neurological disorders involved in neuropathy evaluation
  • Cognitive or reading disorders to prevent the questionnaires from being filled
  • People with musculoskeletal or orthopedic disorders that affect exercise will not be included.

Outcomes

Primary Outcomes

Visual Analog Scale

Time Frame: six week

visual analogue scale measures pain on a horizontal 100mm line. The most left side on this line is defined no pain and the most right side is defined as 'the most severe pain imaginable'. Patients mark a point on the line according to the pain they feel. The pain level is measured in millimeters from the left to the marked point. we evaluate the current pain, the usual pain in the last month, the worst pain in the last month.

Secondary Outcomes

  • Short Pain Inventory(six week)
  • Neuropathic Pain Impact on Quality of Life questionnaire(six week)
  • Neuropathic Pain Scale(six week)

Study Sites (1)

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