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Neuromuscular Electrical Stimulation in Patients With Idiopathic Pulmonary Fibrosis

Primary Purpose

Idiopathic Pulmonary Fibrosis, Neuromuscular Electrical Stimulation

Status
Recruiting
Phase
Not Applicable
Locations
Turkey
Study Type
Interventional
Intervention
Aerobic exercise
Neuromuscular electrical stimulation
Sponsored by
Biruni University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Idiopathic Pulmonary Fibrosis focused on measuring pulmonary rehabilitation, neuromuscular electrical stimulation

Eligibility Criteria

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

Inclusion Criteria:

  • A diagnosis of IPF according to current ATS / ERS guidelines has been followed by a pulmonary specialist for at least 6 months
  • Patients who are clinically stable, have no flare or infection.

Exclusion Criteria:

  • Orthopedic and neurological problems that may interfere with exercise training,
  • Modification of medical treatment during the study,
  • Unstable cardiac diseases,
  • Participation in another pulmonary rehabilitation program over the past 12 months,
  • Inadequate cooperation,
  • Contraindications for the application of neuromuscular electrical stimulation (risk of embolism, neoplasm, infection in the region of application, pacemaker, sensory defect).

Sites / Locations

  • Istanbul UniversityRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Sham Comparator

Experimental

Arm Label

Sham group

NMES group

Arm Description

Following the assessments, sham group will participate in a 20-30 minute low-medium intensity aerobic exercise training with cycling ergometer. In Sham training group, NMES will be applied to the same region after aerobic exercise, current frequency is 5 Hz, current transit time is 300 μs, 10 seconds warning, 30 seconds electrical stimulation in 20 seconds rest period. The rehabilitation program will be administered two days a week for 8 weeks under the supervision of a physiotherapist.

Following the assessments, both groups will participate in a 20-30 minute low-medium intensity aerobic exercise training with cycling ergometer. After the aerobic exercise in NMES group, bilateral NMES application on Quadriceps femoris muscle will be applied as symmetrical biphasic square wave current with a wave frequency of 35-60 Hz, phase transition time of 8 seconds and active resting time of 15 seconds.

Outcomes

Primary Outcome Measures

Assessment of exercise capacity
Exercise capacity will be assessed with 6-minutes walk test. The six minutes walking distance will be recorded in "metres".
Assessment of endurance capacity
Endurance capacity will be assessed with "Shuttle Endurance Walking test". The number of shuttles will be recorded and maximum VO2 will be calculated.

Secondary Outcome Measures

Assessment of peripheral muscle strength
Peripheral muscle strength will be assessed with hand held dynamometer for quadriceps muscles.
Assessment of fatigue
Fatigue will be assessed with Fatigue Severity Scale. The scale consists 9 questions. The minimum score is 0 and maximum score is 63. Higher scores indicate worse fatigue level.
Assessment of activities of daily living
The activities of daily living will be assessed by "The London Chest Daily Activities of Daily Living Questionnaire. The scale has 4 subgroups; self-care (4 question), about home (six question), physical activity (2 question) and leisure time (3 question). The minimum score is 0 and maximum score is 75. Higher scores indicate worse conditions.
Assessment of quality of life: "Saint George Quality of Life Survey
The quality of life will be assessed by "Saint George Quality of Life Survey". The scale consists 50 questions. The minimum score is 0 and the maksimum score is 100. Higher scores indicate poor quality of life.

Full Information

First Posted
March 13, 2019
Last Updated
May 11, 2023
Sponsor
Biruni University
Collaborators
Istanbul University - Cerrahpasa (IUC), Istanbul University
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1. Study Identification

Unique Protocol Identification Number
NCT03890250
Brief Title
Neuromuscular Electrical Stimulation in Patients With Idiopathic Pulmonary Fibrosis
Official Title
Investigation of the Effectiveness of Neuromuscular Electrical Stimulation in Patients With Idiopathic Pulmonary Fibrosis
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Recruiting
Study Start Date
March 20, 2019 (Actual)
Primary Completion Date
November 1, 2023 (Anticipated)
Study Completion Date
December 1, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Biruni University
Collaborators
Istanbul University - Cerrahpasa (IUC), Istanbul University

4. Oversight

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

5. Study Description

Brief Summary
Pulmonary rehabilitation should be initiated and lifelong at the time of diagnosis for patients with IPF. However, the symptoms of the disease and its progression limit clinical options in terms of participation and sustainability in rehabilitation programs. For this purpose, patients with IPF need physiotherapy and rehabilitation options that will not increase the symptoms associated with exercise and contribute to the program in the long term. Neuromuscular electrical stimulation (NMES) is a rehabilitation option that can be applied to specific muscle groups without the ventilator and cardiac load especially in patients who can not actively exercise or have decreased muscle strength. In adult patients with an advanced disease characterized by reduced muscle strength, the use of NMES in addition to aerobic exercise programs is recommended as part of rehabilitation programs. In the literature, no studies investigating the efficacy of NMES have been found in individuals with IPF or interstitial lung disease. NMES application in addition to aerobic exercise seems to be a reasonable option when considering the symptoms of patients with IPF and the progression of the disease. The aim of this project is to investigate the efficacy of NMES in addition to aerobic exercise in IPF patients based on evidence by objective methods.
Detailed Description
Idiopathic pulmonary fibrosis (IPF) is a progressive, fibrotic interstitial lung disease characterized by progressive dyspnoea, reduced exercise capacity, quality of life, and classified as a rare disease. With the increase in medical treatment options, the progression of the disease slows down. Increased time of survival has increased the need for pulmonary rehabilitation programs that have been shown to be effective in patients' exercise capacity, participation in daily living activities, and improvement in the quality of life. Patients with IPF have been shown to be able to improve dyspnoea, fatigue, exercise capacity, daily living activities and quality of life with home-based or supervised breathing, posture, strengthening and aerobic/endurance exercise programs. Pulmonary rehabilitation should be initiated and lifelong at the time of diagnosis for patients with IPF. However, the symptoms of the disease and its progression limit clinical options in terms of participation and sustainability in rehabilitation programs. For this purpose, patients with IPF need physiotherapy and rehabilitation options that will not increase the symptoms associated with exercise and contribute to the program in the long term. Neuromuscular electrical stimulation (NMES) is a rehabilitation option that can be applied to specific muscle groups without the ventilator and cardiac load especially in patients who can not actively exercise or have decreased muscle strength. In adult patients with an advanced disease characterized by reduced muscle strength, the use of NMES in addition to aerobic exercise programs is recommended as part of rehabilitation programs. In the literature, no studies investigating the efficacy of NMES have been found in individuals with IPF or interstitial lung disease. NMES application in addition to aerobic exercise seems to be a reasonable option when considering the symptoms of patients with IPF and the progression of the disease. The aim of this project is to investigate the efficacy of NMES in addition to aerobic exercise in IPF patients based on evidence by objective methods.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Idiopathic Pulmonary Fibrosis, Neuromuscular Electrical Stimulation
Keywords
pulmonary rehabilitation, neuromuscular electrical stimulation

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Thirty IPF patients aged 40-80 years who are followed up at Istanbul University, Istanbul Medical Faculty Chest Disease Department will include in the study. Participants will be divided into two groups as the NMES group and the Sham Training Group, using a computer-assisted randomization table.
Masking
ParticipantInvestigatorOutcomes Assessor
Masking Description
The assessor will be blind to the randomization and the investigator will be blind to the results of assessments.
Allocation
Randomized
Enrollment
30 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Sham group
Arm Type
Sham Comparator
Arm Description
Following the assessments, sham group will participate in a 20-30 minute low-medium intensity aerobic exercise training with cycling ergometer. In Sham training group, NMES will be applied to the same region after aerobic exercise, current frequency is 5 Hz, current transit time is 300 μs, 10 seconds warning, 30 seconds electrical stimulation in 20 seconds rest period. The rehabilitation program will be administered two days a week for 8 weeks under the supervision of a physiotherapist.
Arm Title
NMES group
Arm Type
Experimental
Arm Description
Following the assessments, both groups will participate in a 20-30 minute low-medium intensity aerobic exercise training with cycling ergometer. After the aerobic exercise in NMES group, bilateral NMES application on Quadriceps femoris muscle will be applied as symmetrical biphasic square wave current with a wave frequency of 35-60 Hz, phase transition time of 8 seconds and active resting time of 15 seconds.
Intervention Type
Other
Intervention Name(s)
Aerobic exercise
Intervention Description
A 20-30 minutes low-medium intensity aerobic exercise training with cycling ergometer.
Intervention Type
Other
Intervention Name(s)
Neuromuscular electrical stimulation
Intervention Description
Bilateral NMES application on Quadriceps femoris muscle will be applied as symmetrical biphasic square wave current with a wave frequency of 35-60 Hz, phase transition time of 8 seconds and active resting time of 15 seconds
Primary Outcome Measure Information:
Title
Assessment of exercise capacity
Description
Exercise capacity will be assessed with 6-minutes walk test. The six minutes walking distance will be recorded in "metres".
Time Frame
2 months
Title
Assessment of endurance capacity
Description
Endurance capacity will be assessed with "Shuttle Endurance Walking test". The number of shuttles will be recorded and maximum VO2 will be calculated.
Time Frame
2 months
Secondary Outcome Measure Information:
Title
Assessment of peripheral muscle strength
Description
Peripheral muscle strength will be assessed with hand held dynamometer for quadriceps muscles.
Time Frame
2 months
Title
Assessment of fatigue
Description
Fatigue will be assessed with Fatigue Severity Scale. The scale consists 9 questions. The minimum score is 0 and maximum score is 63. Higher scores indicate worse fatigue level.
Time Frame
2 months
Title
Assessment of activities of daily living
Description
The activities of daily living will be assessed by "The London Chest Daily Activities of Daily Living Questionnaire. The scale has 4 subgroups; self-care (4 question), about home (six question), physical activity (2 question) and leisure time (3 question). The minimum score is 0 and maximum score is 75. Higher scores indicate worse conditions.
Time Frame
2 months
Title
Assessment of quality of life: "Saint George Quality of Life Survey
Description
The quality of life will be assessed by "Saint George Quality of Life Survey". The scale consists 50 questions. The minimum score is 0 and the maksimum score is 100. Higher scores indicate poor quality of life.
Time Frame
2 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: A diagnosis of IPF according to current ATS / ERS guidelines has been followed by a pulmonary specialist for at least 6 months Patients who are clinically stable, have no flare or infection. Exclusion Criteria: Orthopedic and neurological problems that may interfere with exercise training, Modification of medical treatment during the study, Unstable cardiac diseases, Participation in another pulmonary rehabilitation program over the past 12 months, Inadequate cooperation, Contraindications for the application of neuromuscular electrical stimulation (risk of embolism, neoplasm, infection in the region of application, pacemaker, sensory defect).
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Buket Akıncı, Assist.Prof
Phone
+90 5056415692
Email
barbuket@hotmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Buket Akıncı, Assist.Prof.
Organizational Affiliation
Biruni University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Istanbul University
City
Istanbul
Country
Turkey
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Buket Akıncı, Assist.Prof
Phone
+ 90 5056415692
Email
barbuket@hotmail.com
First Name & Middle Initial & Last Name & Degree
Goksen Kuran Aslan, Assoc.Prof
Phone
+ 90 5324095246
Email
goksenkuran@hotmail.com
First Name & Middle Initial & Last Name & Degree
Ozge Ertan, PT
First Name & Middle Initial & Last Name & Degree
Goksen Kuran Aslan, Assoc.Prof
First Name & Middle Initial & Last Name & Degree
Nigar Gulfer Okumus, Prof.Dr.

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
24293474
Citation
Holland AE, Wadell K, Spruit MA. How to adapt the pulmonary rehabilitation programme to patients with chronic respiratory disease other than COPD. Eur Respir Rev. 2013 Dec;22(130):577-86. doi: 10.1183/09059180.00005613.
Results Reference
result
PubMed Identifier
27748503
Citation
Jones S, Man WD, Gao W, Higginson IJ, Wilcock A, Maddocks M. Neuromuscular electrical stimulation for muscle weakness in adults with advanced disease. Cochrane Database Syst Rev. 2016 Oct 17;10(10):CD009419. doi: 10.1002/14651858.CD009419.pub3.
Results Reference
result

Learn more about this trial

Neuromuscular Electrical Stimulation in Patients With Idiopathic Pulmonary Fibrosis

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