Lung Diseases Clinical Trial
Official title:
Effects of Transcutaneous Nerve Electrostimulation (TENS) of Acupuncture Points on Pulmonary Function and Dyspnea Symptoms in Patients With Pulmonary Nodules Treated at a Referral Service: A Randomized Single Blind Study
The ancient use of acupuncture as a treatment modality of traditional Chinese medicine has
also been proven effective in Western medicine. The use of this treatment tool for pain
control is already proven in the literature and today is considered an important adjuvant for
this purpose. However, the ancient texts of acupuncture also report the use of certain points
to tonify organs functions, despite of pain control. According to these texts there are some
points that allow the treatment of lung diseases improving respiratory function.
In order to investigate the effects of stimulation of such points using electric field
application, the effect of these procedure on pulmonary function and the impact of this
practice on dyspnea symptoms, the investigators will conduct a randomized study with 60
patients (1: 1 randomization) distributed in 2 arms (intervention arm-BI and control arm-BC).
Transcutaneous neural stimulation of acupuncture points of the BI patients will be performed.
For the BC arm the investigators will place the electrodes over the points without turn on
the device to produce a placebo effect. Pulmonary function test, Borg scale application and 6
min walk test will be performed before and after the intervention in each group for
subsequent data comparison.
Introduction:
The use of acupuncture for pain management is well defined and fully established. The
stimulation of acupuncture points using needles, electrical stimuli, thermal or laser stimuli
produce local effects at the point (nociceptor stimulation and release of inflammatory
mediators) that generate systemic effects (serotonin release and endorphins in the Central
Nervous System). leading to the state of body relaxation, well-being, changes in heart rate,
blood pressure and analgesia.
However, acupuncture can trigger other effects beyond pain control. In ancient texts dealing
with the subject there are descriptions of points capable of promoting improvement of
specific organic functions such as pulmonary function. 2 This effect is due to changes
generated by the action of acupuncture on the autonomic nervous system promoting
bronchodilation and decreased mucus production. Some studies of effects of acupuncture in
patients with chronic obstructive pulmonary disease have shown promising results related to
improved lung function and reduced symptoms.
Transcutaneous nerve electrostimulation (TENS) can be used to stimulate acupuncture points as
an alternative to needles. This modality of stimulation prevents the occurrence of serious
complications such as pneumothorax secondary to needle application to thoracic points. This
practice turns the procedure safer allowing any trainned healthcare professional to do it.
Goals:
1. Evaluate the immediate effects of this procedure on pulmonary function.
2. Evaluate the effects of TENS on dyspnea symptoms.
Materials and methods:
Will be recruited 60 participants over the age of 18 years, smokers and patients with
pulmonary nodules attended at Santa Marcelina Hospital. Patients with pacemakers, patients
unable to read, understand and sign the informed consent form, with mobility restrictions,
chest pain and patients who have previously used TENS will be excluded from this study.
Participants will be randomized in a 1/1 ratio to form 2 arms: intervention arm (BI) and
control arm (BC).
The BI participants will initially undergo simple spirometry and a 6-minute walk test and
Borg scale application (this texts are detailed at "Tests Description" item at the end of
this manuscript) upon admission to the thoracic surgery department. Immediately after the
exams, they will undergo to a TENS application session over the acupuncture points: Feishu,
Zhongfu, Taiyuan and Dingchuan using a frequency of 200Hz and a pulse time of 80 seconds of
sufficient intensity to cause a slight sensation of local numbness without muscle
fasciculations. The TENS application time will be 30 minutes. Immediately after the TENS
application, the participants will be submitted to a new spirometry, a new 6-minute walk test
and again to the Borg scale evaluation.
The BC participants will undergo to the same steps as BI, however when applying TENS to these
participants the investigators will place the electrodes over the points without turning on
the device in order to obtain the effect of a placebo. To minimize the impact of non-blinding
investigators, will be designated a specific investigator who will be responsible for
randomizing participants at the time of TENS application and performing the intervention do
not allowing the investigators responsible for data collection know whether the patient will
be BI or BC. After data collection, the same investigator will segregate the information from
BC and BI keeping the subgroups identification in secret do not allowing the investigator who
will perform the statistical analysis know what are the groups. Once the data analysis is
ready, the investigator responsible for randomization will tell the other investigators which
subgroup corresponds to each arm.
Tests Description:
# 6-minute Walk Test (6 MWT):
In 2002, the American Thoracic Society (ATS) published guidelines on how to perform the 6
MWT. This guideline stressed the need for a standardized protocol to perform the 6 MWT to
minimize variation in results.
Although the 6 MWT is very safe, emergency equipment should be at hand. The test should be
conducted by personnel qualified to use this equipment. Physicians are not required to be
present in most situations, but should be readily available. The physician ordering the test
may decide if a physician should supervise the test.
According to ATS guidelines, a 30 meters distance course is recommended. Turnaround points
should be identified. Three-meter interval measurements are marked with colored tape on the
floor. Shorter corridor lengths may increase the 6 MWD due to more frequent turns involved.
Required equipment
1. Stop watch or timer
2. Two small cones to mark the lap boundaries
3. Measurement scale for floor measurement
4. Mechanical lap counter
5. Resuscitation equipment
The 6 MWT is performed on a walking track in hospital facility. The track has been marked at
3-m intervals so that accurate measurement of the walking distance can be performed. Chairs
are available at 30-m intervals in case the patients become so symptomatic that have to stop
and sit.
Patient preparation
1. Comfortable clothing should be worn
2. Environment temperature should be ambient
3. Shoes should be comfortable and any walking aids that the patient ordinarily uses should
be used
4. Light meals are acceptable before morning and afternoon tests
Technique
1. Don't perform a warm up before the test.
2. The patient should rest comfortably for 10 minutes prior to the test. During this time
blood pressure and heart rate should be measured and potential contraindications
assessed.
3. Pulse oximetry is optional. If it is used, it should be ensured that readings are stable
prior to starting the 6 MWT, and signal is optimized.
4. Before the test starts, the patient should stand up and rate for dyspnea and fatigue.
The Borg scale may be used for this.
5. Set the lap counter to zero and timer to 6 minutes. Assemble all necessary equipment and
move to starting point.
6. The supervisor may walk a lap to demonstrate performance of the test to the patient.
During the test the supervisor should never walk with or in front of the patient as the
patient may try to match the supervisor's pace. The supervisor may walk behind the
patient to support the patient in case of staggering or to prevent falling. The patient
is allowed to rest during the test if gets fatigued.
7. Use standardized phrases and an even tone for encouragement at completion of each minute
of the test. For an example of a standardized script, the reader is referred to the 2002
ATS guidelines. Some examples are "keep up the good work" or "you are doing fine".
8. Resting during the test is allowed, but don't stop the clock. If the patient cannot go
any further, the test should be stopped and distance covered recorded.
9. Stop the test if patient develops chest pain, intolerable dyspnea, staggering,
diaphoresis, intolerable cramps, and/or ashen appearance. Test supervisors should be
trainned to provide appropriate care at this point.
10. At the conclusion of the test, ask the patient to rate his/her dyspnea and fatigue
levels. Record the reason for stopping the test.
Additional details about technique
1. If the patient is on supplemental oxygen, use the same oxygen level that normally uses
with exercise.
2. The 2002 ATS guidelines do not recommend routine measurement of pulse oximetry during
the test. In untreated patients with pulmonary hypertension, oxygen desaturation >10%
during 6 MWT has been associated with mortality. With the widespread availability of
light-weight portable oximeters, monitoring of oxygen saturation during walking can be
reliably performed.
3. Quality control and standardization are important to reduce variability in measurement.
Persons supervising the test should be trained using a standard protocol, and should
conduct supervised 6 MWTs before patients are able to perform them independently. A
practice test generally should not be needed. If a practice test is done, there should
be a wait time of about an hour between the two tests, and the longer 6 MWD should be
reported.
- Borg scale measure:
The scale allows individuals to subjectively rate their level of exertion during exercise or
exercise testing.
It is a gradual scale that varies from zero (no fatigue symptoms) to ten (maximum fatigue
like the sensation of the hardest race that the participant have ever did)
Patients with higher values on Borg scale evaluation are considered worse.
see the link of Borg scale at the references.
;
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT05563701 -
Evaluation of the LVivo Image Quality Scoring (IQS)
|
||
Completed |
NCT04908397 -
Carnitine Consumption and Augmentation in Pulmonary Arterial Hypertension
|
Phase 1 | |
Terminated |
NCT03309358 -
A Study of the Safety and Tolerability of Inhaled SNSP113 in Healthy Subjects and Subjects With Stable Cystic Fibrosis
|
Phase 1 | |
Completed |
NCT03682354 -
ESPB Versus INB With PCIA in Video-assisted Thoracic Surgery
|
N/A | |
Enrolling by invitation |
NCT03683186 -
A Study Evaluating the Long-Term Efficacy and Safety of Ralinepag in Subjects With PAH Via an Open-Label Extension
|
Phase 3 | |
Completed |
NCT03626519 -
Effects of Menthol on Dyspnoea in COPD Patients
|
N/A | |
Recruiting |
NCT06004440 -
Real World Registry for Use of the Ion Endoluminal System
|
||
Completed |
NCT04874948 -
Absorption, Elimination and Safety of 14C-labeled Radioactive BTZ-043, a New Compound in TB Treatment
|
Phase 1 | |
Completed |
NCT02926768 -
Phase I/II Study of CK-101 in NSCLC Patients and Other Advanced Solid Tumors
|
Phase 1 | |
Completed |
NCT01443845 -
Roflumilast in Chronic Obstructive Pulmonary Disease (COPD) Patients Treated With Fixed Dose Combinations of Long-acting β2-agonist (LABA) and Inhaled Corticosteroid (ICS)
|
Phase 4 | |
Completed |
NCT00281216 -
Innate and Adaptive Immunity in Individuals Experiencing Chronic Obstructive Pulmonary Disease Exacerbations
|
N/A | |
Terminated |
NCT00233207 -
IC14 Antibodies to Treat Individuals With Acute Lung Injury
|
Phase 2 | |
Completed |
NCT00269256 -
Stress, Environment, and Genetics in Urban Children With Asthma
|
N/A | |
Recruiting |
NCT00129350 -
Assessment of Heart and Heart-Lung Transplant Patient Outcomes Following Pulmonary Rehabilitation
|
Phase 1 | |
Active, not recruiting |
NCT00115297 -
Montelukast for Early Life Wheezing
|
Phase 2/Phase 3 | |
Completed |
NCT00094276 -
Intervention for Improving Asthma Care for Minority Children in Head Start
|
N/A | |
Completed |
NCT00091767 -
Genetic Studies in Difficult to Treat Asthma: TENOR
|
N/A | |
Completed |
NCT00069823 -
Study of Acid Reflux in Asthma
|
Phase 3 | |
Completed |
NCT00233168 -
Effectiveness of Public Health Model of Latent Tuberculosis Infection Control for High-Risk Adolescents
|
N/A | |
Completed |
NCT00089752 -
Continuous Positive Airway Pressure to Improve Milder Obstructive Sleep Apnea
|
N/A |