AzTrials
AzTrials

InsomniaNCT05426226

Effect of Low Level Light Irradiation on Insomniacs' Meridians During the First Sleep Cycle.

A study testing laser acupuncture in people with Insomnia, run by Taipei Veterans General Hospital, Taiwan at 1 site in Taiwan.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
Search all trials

Trial summary

Introduction In the past, it was found that stimulating the meridians and acupoints with low-level light often had a good effect. However, for safety reasons, most instruments such as laser acupuncture devices still need to be used by medical personnel, and it is difficult to apply to insomnia patients at bed-time or… Read more about this study

Who is it for?
Ages 20 to 65 yearsHealthy volunteers can take part
Conditions the study is for
Insomnia
What is being tested?
laser acupuncture
Type of treatment
Medical device
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
120 participants
Where
1 siteTaiwan
Study dates
10 Aug 2022to 30 May 2024
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 20 to 65 years
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • aged 20 to 65 years
  • No sleep pills for 3 months
  • Body Mass Index (BMI) : 18.5-30
  • Blood pressure: within normal range (140 mmHg/90 mmHg)
  • People with regular wake-up time
  • The bedtime is between 22:00 and 2:00.

Who cannot join

  • People with sleep disorders other than insomnia
  • those currently taking drugs;
  • with cardiovascular disease, cancer, psychiatric disease, kidney disease, diabetes, chronic disease and physical discomfort
  • Exclude tobacco, alcohol, caffeine, and drug addicts
  • Exclude from fitzpatrick skin type classification - V and VI (skin is black and dark brown)
  • People whose skin is allergic to light (light sensitivity, solar dermatitis).

Trial locations and contacts

1 site in 1 country.

Taiwan1 site
  • Center for Traditional Medicine, Taipei Veterans General Hospital

    Taipei, 112

    Yuan-Pu Tseng, MD, 886-2-28757453 ext. 230, m061j3@gmail.com

Other trials in Taiwan

About this study

Introduction In the past, it was found that stimulating the meridians and acupoints with low-level light often had a good effect. However, for safety reasons, most instruments such as laser acupuncture devices still need to be used by medical personnel, and it is difficult to apply to insomnia patients at bed-time or the first sleep cycle, these two periods have a considerable impact on sleep quality.

Therefore, the purpose of this study is to provide a safer wearable light-therapy device for Insomnia patients, so that it can be used in home sleep situations, and the improvement of subjects' sleep qualtity and meridian energy will be evaluated by PSG, HRV parameters, sleep questionnaires, and Ryodoraku value (reflects the meridian electric resistance).

Methods Aim1: To evaluate whether the subjects are more relaxed by observing the changes in heart rate and meridian energy of healthy subjects after low-level light irradiating to Shenmen, Daling, Neiguan (acupoints for insomnia). We also consider the difference of light source and the skin color in experiment design. Aim2: To assess whether the insomnia patients' sleep quality has improved after applying the wearable light therapy device to subjects' bed-time (include the first sleep cycle). We use PSG, sleep questionnaires, stroop test for evaluation.

Read the detailed description

Hypotheses and Aims

In the past, there are no studies on using light acupuncture during the first sleep cycle or bed-time. So, we have the following hypotheses: First, irradiating low level light on the sleep acupoints during these periods will strengthen the activity of the parasympathetic during these periods; Second, the activity of the parasympathetic will improve the quality of sleep in the first sleep cycle, because the parasympathetic activity of sleep onset(SO) is an indicator of sleep quality; Third, the improvement of sleep quality in the first sleep cycle will affect the quality of total sleep and daytime cognitive functions. I divide the research hypotheses for details into three categories:

Part 1: To observe the relationship between light stimulation of traditional Chinese medicine (TCM) sleep-aiding acupoints.

Hypothesis 1-1: After the laser stimulates the sleep-aiding acupoints, the energy of the meridian that is too high will decrease, and the energy of the meridian that is too low will increase.

Hypothesis 1-2: After laser acupuncture, the qi of the meridians will not be consumed too quickly like acupuncture, so the needle retention is safe.

Hypothesis 1-3: The efficacy of LED stimulation of acupoints should be similar to that of laser acupuncture.

Part 2: Assumptions Related to Optical Design:

Hypothesis 2-1: The most suitable light specifications for dark-skinned people are different from light-skinned people.

Hypothesis 2-2: Some new optical components have good performance in light transmission Hypothesis 2-3: The newly designed light penetration experiment can obtain optical parameters more accurately and quickly

Part 3: Heart Rate Variability and Sleep Improvement:

Hypothesis 3-1: We could improve parameters of heart rate variability by using the wearable light therapy device.

Hypothesis 3-2: Optimizing HRV parameters before going to bed can improve the quality of the first sleep cycle.

Hypothesis 3-3: After using a wearable light therapy device to improve the first sleep cycle, it can also enhance the whole night sleep quality.

Hypothesis 3-4: Improved sleep quality from using wearable light therapy device can lead to the improvements in daily cognitive function.

Significance If this study is successfully proved to improve the sleep quality of insomnia patients, it will give insomnia patients a treatment option other than sleep pills, make light therapy be widely applied to the home environment, and make researchers pay more attention to the possibility of using TCM procedure in the first sleep cycle.

Research Materials and Equipment Research Methods

STAGE 1:

Participant

Experiment A:

A preliminary experiment of "laser acupuncture" on sleep acupoints (healthy subjects).

Subjects: 30 healthy subjects.

Designs

Experimental procedure:

  1. The experiments will be carried out twice, once with laser intervention, and once with sham. The experiment time was 25 minutes, and both were scheduled between 3:30 and 5:00 PM. The room temperature was controlled between 25-27 degrees. The interval between two experiments is between one to two weeks to avoid the influence of seasonal factors.
  2. Before the experiment, the subjects' Ryodoraku value will be measured. The subjects shall sit in a fixed posture and step on the square box at room temperature and avoid touching metal or cold materials.
  3. Before the start of the experiment, ask the subject to hold the hand-held heart rate measurement device and teach him how to use it; set up the laser acupuncture head on the sleep acupoints we used; then blindfold him with a blinder.
  4. From 0 to 5 minutes, let the subject measure the first HRV parameters as the data [before intervention].
  5. From the 5th to 10th minute of the experiment, the laser or sham intervenes at the eighth minute, and the intervention time lasts for ten minutes.
  6. From the 10th to 15th minute, the subject measured the second time HRV parameters, which was used as the data of the [during the intervention].
  7. In the 15th to 20th minutes, the laser or sham will end the intervention at the 17th to 18th minutes.
  8. From the 20th to 25th minute of the experiment, the subject measured the third heart rate variability parameters under blindfolded conditions, as the data of the [after the intervention].
  9. Take off his blinder, Ask the subject to measure Ryodoraku value again, and end the experiment.
  • Sham intervention method: The subject in blindfolded state can hear the same prompt sound as laser acupuncture, but does not irradiate light. (Fig.3-4)

Experiment B: All procedures are the same as Experiment A, but the light source is change to LED wearable devices. (Fig.5-6)

STAGE 2:

Participant Subjects: 120 insomnia subjects. (80 subjective insomnia; 40 objective insomnia)

Designs

Experimental procedure:

Prepare period:

  1. Inform the subjects of the research process, complete questionnaire such as PSQI, MEQ, ISI, ESS, and limb motor sensory survey to determine whether they are eligible for the study.
  2. The subject fills in the sleep diary for one week and wears an oximeter to confirm that there is no sleep abnormality.
  3. The subject used a tiny wireless sleep physiological recorder to record the quality of sleep for two nights. The first night was the adaptation period and was not included in the analysis, and the sleep data of the second night was included in the analysis (base line).

Experimental period:

  1. DAY0: The subjects were randomly assigned to group A and group B, the group A will take light acupuncture in the first month, and sham in the next month; Group B is opposite.
  2. DAY1: The subject filled out the rest of the questionnaires, and then asked them to complete the Ryodoraku measurement, and wear the TD1 tiny PSG recorder to perform the first multi-channel physiological measurement, explain the use process of the wearable light therapy deivce, and let them download the EncephalApp stroop test Program.
  3. DAY15: All procedures are the same as DAY1, but no questionnaires. (second tiny PSG record)
  4. DAY30: All procedures are the same as DAY1, fill questionnaires like PSQI, ISI etc. (third tiny PSG record)
  5. DAY31-DAY36: take a break and do nothing.(wash-out)
  6. DAY37: All procedures are the same as DAY1. (fourth tiny PSG record)
  7. DAY52: All procedures are the same as DAY15. (fifth tiny PSG record)
  8. DAY67: All procedures are the same as DAY30. (sixth tiny PSG record)
  9. DAY68: The subject returned the wearable light therapy device and TD1 recorder, and confirmed whether the data of TD1 is complete. (Fig. 7)

Analysis Methods The main data is expressed in terms of mean and standard deviation (SD). The before -after difference in same groups is analyzed by t-test, and the difference between groups is also analyzed by ANOVA.

Conditions
Insomnia
Being tested
laser acupuncture, sham device
Keywords
Heart rate variability, meridian, insomnia
Medical subject headings
Sleep Initiation and Maintenance Disorders

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • laser acupunctureDevice

    using laser acupuncture device on sleep acupoints during sleep

  • sham deviceDevice

    using sham device on sleep acupoints during sleep

Study groups in NCT05426226
Study groupRoleWhat they receive
laser groupActive comparatorLaser group use specific wavelength to light the sleep acupoints during. If the laser group take light acupuncture in the first month, and then become the sham group in the next month, vice versa.
Receives: Device: laser acupuncture
sham groupSham comparatorsham group use the same divce and acupointsas the laser group, but the light is just a regular light. If the laser group take light acupuncture in the first month, and then become the sham group in the next month, vice versa.
Receives: Device: sham device

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Differences in sleep EEG before and after the laser irradiation compared to the sham group

    According to sleep EEG,we can analysis participants' brain waves (alpha,beta,theta,delta) and sleep stages,etc. to evaluate their objective sleep quality

    Measured: Change from Baseline sleep EEG at 67 days

  2. Differences in Heart rate variability before and after the laser irradiation compared to the sham group

    HRV is measured by the variations in the R-R interval between the successive peaks of the QRS complex in the ECG wave. Based on fast Fourier transform, time-domain (R-R interval) transfer to frequency domain resulting total power (TP, 0.04-0.15), low frequency (LF, 0.06-0.6Hz), high frequency (HF, 0.6-2.4Hz), normalized LF (LF%) and LF/HF ratio are obtained. LF% and HF represent an index of sympathetic activity and parasympathetic activity respectively. LF/HF is indicative of the sympathetic to parasympathetic autonomic balance.

    Measured: Change from heart rate variability parameters at 67 days

Secondary outcomes (8)
  1. Differences in the Epworth Sleepiness Scale (ESS) before and after the laser irradiation compared to the sham group.

    The Epworth Sleepiness Scale is widely used in the field of sleep medicine as a subje

    Measured: Change from Baseline ESS at 67 days

  2. Differences in Visual Analogue Scale (VAS) before and after the laser irradiation compared to the sham group.

    Visual Analogue Scale (VAS) consists of a line, 10 cm in length. Individuals point to or mark a spot on the line where they feel indicates their current their emotion, fatigue level and sleep quality. The score of emotion level is from 0cm (very nervous) to 10 cm (very relaxing). The score of fatigue level is from 0 cm (very energetic) to 10 cm (very sleepy). The score of sleep quality is from 0 cm (poor) to 10 cm (sleep well). The maximum total score is 100% (equal 10cm).

    Measured: Change from Baseline VAS at 67 days

  3. Differences in scores of stroop test before and after the laser irradiation compared to the sham group.

    The Visual Stroop Test is designed to assess cognitive flexibility and attention span by examining a patient's ability to separate word and color naming stimuli through the use of three separate subtests.

    Measured: Change from Baseline score of stroop at 67 days

  4. Differences in the Insomnia Severity Index (ISI) before and after the laser irradiation compared to the sham group.

    Designed as a brief screening tool for insomnia, the seven-item questionnaire asks respondents to rate the nature and symptoms of their sleep problems using a Likert-type scale. Responses can range from 0 to 4, where higher scores indicate more acute symptoms of insomnia.The maximum total score is 28.

    Measured: Change from Baseline ISI at 67 days

  5. Differences in the Pittsburgh sleep quality index before and after the laser irradiation compared to the sham group.

    The Pittsburgh Sleep Quality Index (PSQI) is a self-report questionnaire that assesses sleep quality over a 1-month time interval. The measure consists of 19 individual items, creating 7 components that produce one global score, and takes 5-10 minutes to complete.The maximum total score is 21. A higher score reflects more poor sleep quality.

    Measured: Change from Baseline PSQI at 67 days

  6. Differences in The Beck Depression Inventory II (BDI-II) before and after the laser irradiation compared to the sham group.

    The Beck Depression Inventory II (BDI-II) is a 21-item, self-rated scale that evaluates key symptoms of depression. It rated on a 4-point scale ranging from 0 to 3 based on severity of each item. The maximum total score is 63. A higher score reflects greater symptoms of depression.

    Measured: Change from Baseline BDI-II at 67 days

  7. Differences in Beck Anxiety Inventory (BAI) before and after the laser irradiation compared to the sham group.

    the Beck Anxiety Inventory (BAI) is a 21-item, self-rated scale that evaluates anxiety levels , rated on a scale from 0 to 3. Each item is descriptive of subjective, somatic, or panic-related symptoms of anxiety.The maximum total score is 63.A higher score reflects greater anxiety.

    Measured: Change from Baseline BAI at 67 days

  8. Differences in Chinese 14-item PSS before and after the laser irradiation compared to the sham group.

    The PSS is an 14-item instrument designed to measure the perception of stress in a month . All items are rated on a 5-point Likert scale from 0 (never) to 4 (very often) and seven of them (4, 5, 6, 7, 9, 10, 13) are reverse-scored.

    Measured: Change from Baseline PSS at 67 days

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted21 Jun 2022
  2. Study start10 Aug 2022 (estimated)
  3. Primary completion30 May 2024 (estimated)
  4. Study completion30 May 2024 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Supportive care
Allocation
Randomised
Intervention model
Crossover
Model description
The subjects were randomly assigned to group A and group B, the group A will take light acupuncture in the first month, and sham in the next month; Group B is opposite.
Masking
Triple blind
Who is masked
Participant, Investigator, Outcomes assessor
Enrolment
120 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05426226
Sponsor's protocol ID
IRB 2022-02-027B
Status last verified
Jul 2022
First submitted
16 Jun 2022
Last updated
1 Aug 2022
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing laser acupuncture in people with Insomnia, run by Taipei Veterans General Hospital, Taiwan at 1 site in Taiwan.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 6 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 1 Aug 2022. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Taiwan. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Yuan-Pu Tseng, MD (886-2-28757453 ext. 230, m061j3@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Differences in sleep EEG before and after the laser irradiation compared to the sham group (time frame: Change from Baseline sleep EEG at 67 days). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 1 Aug 2022.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in