search
Back to results

Effect of a Combined Exercise Program on Neuropathic Pain and Perceived Quality of Life in Type 2 Diabetes

Primary Purpose

Diabetes Mellitus, Type 2, Neuropathic Pain, Neuropathy, Diabetic

Status
Active
Phase
Not Applicable
Locations
Mexico
Study Type
Interventional
Intervention
Combined Exercise
Sponsored by
Universidad Autónoma de Yucatán
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diabetes Mellitus, Type 2 focused on measuring Diabetes Mellitus type 2, Neuropathic pain, combined exercise

Eligibility Criteria

35 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Patients with diabetes type 2 Patients with neuropathy Patients with medical treatment Exclusion Criteria: Patients with several limit function Patients with foot ulcer or amputation Patients who are involved in a exercise program already

Sites / Locations

  • Unidad Universitaria de Inserción Social San José Tecoh

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Combined Exercise

Arm Description

Therapeutic exercise program

Outcomes

Primary Outcome Measures

Change from baseline in neuropathic pain on Douleur Neuropathique-4 (DN4) at 8 weeks
The DN4 questionnaire will be used to evaluate neuropathic pain and its characteristics. DN4 for neuropathic pain consists of interview questions and physical tests. It has 10 items grouped into four questions: seven items relating to the pain description (burning, painful cold, electric shocks) and to its associated abnormal sensations (tingling, pins and needles, numbness, itching), and the other three items relating to a brief bedside neurological examination in the painful area (touch hypoaesthesia, pinprick hypoaesthesia and tactile dynamic allodynia). For scoring, 1 is given to each positive and 0 to each negative item (total score range 0-10). The cut-off value for diagnosis of neuropathic pain is a total score of 4.
Change from baseline in pain intensity on Visual Analogue Scale (VAS) at 8 weeks
Pain severity will be assessed using VAS. Each patient will be asked to choose in a perpendicular line on the VAS at the point that signifies the pain severity. The score is ranged 0-10, 0 suggests no pain and 10 suggest severe pain.
Change from baseline in quality of life on the short form-36 questionnaire (SF-36) at 8 weeks
The 36-item questionnaire consists of eight domains (general health, mental health, role emotion, role physical, body pain, social function, physical function and vitality), which can be further aggregated into a physical component score (PCS) and mental component score (MCS). Total score ranges from 0 to 100, 0 indicates the poor quality of life and 100 indicates the best quality of life.

Secondary Outcome Measures

Socio-demographic data
An identification form will be filled out at the beginning of the study that will include socio-demographic information: sex (woman/man), age (years), marital status (single/married/widowed/divorced), educational stage (Primary education/High School/University/Master) and occupation (yes/no). All data will be presented in frequency and percentage.
Clinical data
An identification form will be filled out at the beginning of the study that will include clinical information: presence of type II diabetes, presence of neuropathy, time of diagnosis (years), Glycemic status (A1C percentage), insulin use (yes/no) and medical treatment. All data will be presented in frequency and percentage. For the neurological examination of the extremities, three instruments will be used: the 10g or Semmes-Weinstein monofilament, 128 hertz tuning fork and Taylor reflex hammer.
Weight measurement
Body weight will be measured in kilograms (kg) using the body weight scale "Omron HBF-514C".
Height measurement
Height will be measured in meters (m) using a stadiometer.
Body Mass Index (BMI) measurement
BMI will be calculated by dividing the weight in kilograms by the height in metres squared (kg/m^2).

Full Information

First Posted
December 5, 2022
Last Updated
January 26, 2023
Sponsor
Universidad Autónoma de Yucatán
search

1. Study Identification

Unique Protocol Identification Number
NCT05703152
Brief Title
Effect of a Combined Exercise Program on Neuropathic Pain and Perceived Quality of Life in Type 2 Diabetes
Official Title
Effect of a Combined Therapeutic Exercise Program on Neuropathic Pain and Perceived Quality of Life in Patients With Type 2 Diabetes
Study Type
Interventional

2. Study Status

Record Verification Date
January 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
October 31, 2022 (Actual)
Primary Completion Date
June 30, 2023 (Anticipated)
Study Completion Date
July 31, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Universidad Autónoma de Yucatán

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Therapeutic exercise is one of the therapies used as a treatment for diabetic neuropathy, which is a complication of diabetes. In order to reduce pain and improve the perception of quality of life, a combined therapeutic exercise program will be implemented as an adjuvant and non-pharmacological treatment for diabetic neuropathy.
Detailed Description
This is a prospective, longitudinal, quasi-experimental study of repeated measures (pretest-posttest), has been approved by the research and ethics committee of the Faculty of Medicine of the Autonomous University of Yucatan, issuing a report on October 26, 2022. An identification form will be filled out that will include socio-demographic and clinical data: presence of type II diabetes, presence of neuropathy, sex, age, marital status, schooling, occupation, BMI, time of diagnosis, HbA1C, insulin use, medical treatment and a neurological examination of the extremities. The DN4 questionnaire will be used to evaluate neuropathic pain and its characteristics, the VAS will be used to evaluate the degree of intensity or severity of pain, and the SF-36 questionnaire will be used to evaluate perception before and after the combined exercise program. During the intervention stage, a therapeutic exercise program will be applied that will include two modalities: aerobic and resistance exercise in the facilities of the Unidad Universitaria de Inserción social de San José Tecoh. The duration will be 8 weeks with a frequency of 3 sessions per week, with a duration per session of 60 minutes each, to achieve the minimum total time suggested by the guidelines of 150 minutes per week. These exercises will be prescribed in three phases to increase times, series, repetitions and resistances in a progressive manner according to the Borg scale. For the analysis of the variables, the parametric Student's t-test for related samples or the nonparametric Wilcoxon test with significance at 95% reliability will be used. The implementation of the study can demonstrate significant improvements in the symptomatology of diabetic neuropathy, directly impacting on the perception of the quality of life of patients with type II diabetes.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes Mellitus, Type 2, Neuropathic Pain, Neuropathy, Diabetic
Keywords
Diabetes Mellitus type 2, Neuropathic pain, combined exercise

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
A prospective, longitudinal, quasi-experimental study of repeated measures (pretest-posttest)
Masking
None (Open Label)
Allocation
N/A
Enrollment
12 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Combined Exercise
Arm Type
Experimental
Arm Description
Therapeutic exercise program
Intervention Type
Other
Intervention Name(s)
Combined Exercise
Intervention Description
Therapeutic exercise program will be applied that will include two modalities: aerobic and resistance exercise. The duration will be 8 weeks with a frequency of 3 sessions per week, with a duration per session of 60 minutes.
Primary Outcome Measure Information:
Title
Change from baseline in neuropathic pain on Douleur Neuropathique-4 (DN4) at 8 weeks
Description
The DN4 questionnaire will be used to evaluate neuropathic pain and its characteristics. DN4 for neuropathic pain consists of interview questions and physical tests. It has 10 items grouped into four questions: seven items relating to the pain description (burning, painful cold, electric shocks) and to its associated abnormal sensations (tingling, pins and needles, numbness, itching), and the other three items relating to a brief bedside neurological examination in the painful area (touch hypoaesthesia, pinprick hypoaesthesia and tactile dynamic allodynia). For scoring, 1 is given to each positive and 0 to each negative item (total score range 0-10). The cut-off value for diagnosis of neuropathic pain is a total score of 4.
Time Frame
Baseline and week 8
Title
Change from baseline in pain intensity on Visual Analogue Scale (VAS) at 8 weeks
Description
Pain severity will be assessed using VAS. Each patient will be asked to choose in a perpendicular line on the VAS at the point that signifies the pain severity. The score is ranged 0-10, 0 suggests no pain and 10 suggest severe pain.
Time Frame
Baseline and week 8
Title
Change from baseline in quality of life on the short form-36 questionnaire (SF-36) at 8 weeks
Description
The 36-item questionnaire consists of eight domains (general health, mental health, role emotion, role physical, body pain, social function, physical function and vitality), which can be further aggregated into a physical component score (PCS) and mental component score (MCS). Total score ranges from 0 to 100, 0 indicates the poor quality of life and 100 indicates the best quality of life.
Time Frame
Baseline and week 8
Secondary Outcome Measure Information:
Title
Socio-demographic data
Description
An identification form will be filled out at the beginning of the study that will include socio-demographic information: sex (woman/man), age (years), marital status (single/married/widowed/divorced), educational stage (Primary education/High School/University/Master) and occupation (yes/no). All data will be presented in frequency and percentage.
Time Frame
Before intervention
Title
Clinical data
Description
An identification form will be filled out at the beginning of the study that will include clinical information: presence of type II diabetes, presence of neuropathy, time of diagnosis (years), Glycemic status (A1C percentage), insulin use (yes/no) and medical treatment. All data will be presented in frequency and percentage. For the neurological examination of the extremities, three instruments will be used: the 10g or Semmes-Weinstein monofilament, 128 hertz tuning fork and Taylor reflex hammer.
Time Frame
Before intervention
Title
Weight measurement
Description
Body weight will be measured in kilograms (kg) using the body weight scale "Omron HBF-514C".
Time Frame
Before intervention
Title
Height measurement
Description
Height will be measured in meters (m) using a stadiometer.
Time Frame
Before intervention
Title
Body Mass Index (BMI) measurement
Description
BMI will be calculated by dividing the weight in kilograms by the height in metres squared (kg/m^2).
Time Frame
Before intervention

10. Eligibility

Sex
All
Minimum Age & Unit of Time
35 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with diabetes type 2 Patients with neuropathy Patients with medical treatment Exclusion Criteria: Patients with several limit function Patients with foot ulcer or amputation Patients who are involved in a exercise program already
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Maria Gabriela Aké Palomo
Organizational Affiliation
Facultad de Medicina
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Damaris Francis Estrella Castillo, PhD
Organizational Affiliation
Falcultad de Medicina
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Gloria de los Ángeles Uicab Pool, PhD
Organizational Affiliation
Facultad de Enfermeria
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Hector Armado Rubio Zapata
Organizational Affiliation
Facultad de Medicina
Official's Role
Study Director
Facility Information:
Facility Name
Unidad Universitaria de Inserción Social San José Tecoh
City
Mérida
State/Province
Yucatán
ZIP/Postal Code
97299
Country
Mexico

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
27999003
Citation
Pop-Busui R, Boulton AJ, Feldman EL, Bril V, Freeman R, Malik RA, Sosenko JM, Ziegler D. Diabetic Neuropathy: A Position Statement by the American Diabetes Association. Diabetes Care. 2017 Jan;40(1):136-154. doi: 10.2337/dc16-2042. No abstract available.
Results Reference
background
PubMed Identifier
30586071
Citation
Scholz J, Finnerup NB, Attal N, Aziz Q, Baron R, Bennett MI, Benoliel R, Cohen M, Cruccu G, Davis KD, Evers S, First M, Giamberardino MA, Hansson P, Kaasa S, Korwisi B, Kosek E, Lavand'homme P, Nicholas M, Nurmikko T, Perrot S, Raja SN, Rice ASC, Rowbotham MC, Schug S, Simpson DM, Smith BH, Svensson P, Vlaeyen JWS, Wang SJ, Barke A, Rief W, Treede RD; Classification Committee of the Neuropathic Pain Special Interest Group (NeuPSIG). The IASP classification of chronic pain for ICD-11: chronic neuropathic pain. Pain. 2019 Jan;160(1):53-59. doi: 10.1097/j.pain.0000000000001365.
Results Reference
background
PubMed Identifier
18053212
Citation
Perez C, Galvez R, Huelbes S, Insausti J, Bouhassira D, Diaz S, Rejas J. Validity and reliability of the Spanish version of the DN4 (Douleur Neuropathique 4 questions) questionnaire for differential diagnosis of pain syndromes associated to a neuropathic or somatic component. Health Qual Life Outcomes. 2007 Dec 4;5:66. doi: 10.1186/1477-7525-5-66.
Results Reference
background
PubMed Identifier
32187271
Citation
Pereira EV, Tonin FS, Carneiro J, Pontarolo R, Wiens A. Evaluation of the application of the Diabetes Quality of Life Questionnaire in patients with diabetes mellitus. Arch Endocrinol Metab. 2020 Feb;64(1):59-65. doi: 10.20945/2359-3997000000196. Epub 2020 Mar 13.
Results Reference
background
PubMed Identifier
35029593
Citation
Kanaley JA, Colberg SR, Corcoran MH, Malin SK, Rodriguez NR, Crespo CJ, Kirwan JP, Zierath JR. Exercise/Physical Activity in Individuals with Type 2 Diabetes: A Consensus Statement from the American College of Sports Medicine. Med Sci Sports Exerc. 2022 Feb 1;54(2):353-368. doi: 10.1249/MSS.0000000000002800.
Results Reference
background
PubMed Identifier
30045740
Citation
Pan B, Ge L, Xun YQ, Chen YJ, Gao CY, Han X, Zuo LQ, Shan HQ, Yang KH, Ding GW, Tian JH. Exercise training modalities in patients with type 2 diabetes mellitus: a systematic review and network meta-analysis. Int J Behav Nutr Phys Act. 2018 Jul 25;15(1):72. doi: 10.1186/s12966-018-0703-3.
Results Reference
result

Learn more about this trial

Effect of a Combined Exercise Program on Neuropathic Pain and Perceived Quality of Life in Type 2 Diabetes

We'll reach out to this number within 24 hrs