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

Primary Purpose

Insomnia

Status
Not yet recruiting
Phase
Not Applicable
Locations
Taiwan
Study Type
Interventional
Intervention
laser acupuncture
sham device
Sponsored by
Taipei Veterans General Hospital, Taiwan
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Insomnia focused on measuring Heart rate variability, meridian, insomnia

Eligibility Criteria

20 Years - 65 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • 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.

Exclusion Criteria:

  • 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).

Sites / Locations

  • Center for Traditional Medicine, Taipei Veterans General Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Sham Comparator

Arm Label

laser group

sham group

Arm Description

Laser 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.

sham 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.

Outcomes

Primary Outcome Measures

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
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.

Secondary Outcome Measures

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
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).
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.
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.
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.
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.
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.
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.

Full Information

First Posted
June 16, 2022
Last Updated
July 27, 2022
Sponsor
Taipei Veterans General Hospital, Taiwan
Collaborators
National Yang Ming University
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1. Study Identification

Unique Protocol Identification Number
NCT05426226
Brief Title
Effect of Low Level Light Irradiation on Insomniacs' Meridians During the First Sleep Cycle.
Official Title
Effect of Low Level Light Irradiation on Insomniacs' Meridians During the First Sleep Cycle.
Study Type
Interventional

2. Study Status

Record Verification Date
July 2022
Overall Recruitment Status
Not yet recruiting
Study Start Date
August 10, 2022 (Anticipated)
Primary Completion Date
May 30, 2024 (Anticipated)
Study Completion Date
May 30, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Taipei Veterans General Hospital, Taiwan
Collaborators
National Yang Ming 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
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.
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: 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. 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. 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. From 0 to 5 minutes, let the subject measure the first HRV parameters as the data [before intervention]. 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. 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]. In the 15th to 20th minutes, the laser or sham will end the intervention at the 17th to 18th minutes. 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]. 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: 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. The subject fills in the sleep diary for one week and wears an oximeter to confirm that there is no sleep abnormality. 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: 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. 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. DAY15: All procedures are the same as DAY1, but no questionnaires. (second tiny PSG record) DAY30: All procedures are the same as DAY1, fill questionnaires like PSQI, ISI etc. (third tiny PSG record) DAY31-DAY36: take a break and do nothing.(wash-out) DAY37: All procedures are the same as DAY1. (fourth tiny PSG record) DAY52: All procedures are the same as DAY15. (fifth tiny PSG record) DAY67: All procedures are the same as DAY30. (sixth tiny PSG record) 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Insomnia
Keywords
Heart rate variability, meridian, insomnia

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
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
ParticipantInvestigatorOutcomes Assessor
Masking Description
participants allocation by third party
Allocation
Randomized
Enrollment
120 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
laser group
Arm Type
Active Comparator
Arm Description
Laser 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.
Arm Title
sham group
Arm Type
Sham Comparator
Arm Description
sham 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.
Intervention Type
Device
Intervention Name(s)
laser acupuncture
Intervention Description
using laser acupuncture device on sleep acupoints during sleep
Intervention Type
Device
Intervention Name(s)
sham device
Intervention Description
using sham device on sleep acupoints during sleep
Primary Outcome Measure Information:
Title
Differences in sleep EEG before and after the laser irradiation compared to the sham group
Description
According to sleep EEG,we can analysis participants' brain waves (alpha,beta,theta,delta) and sleep stages,etc. to evaluate their objective sleep quality
Time Frame
Change from Baseline sleep EEG at 67 days
Title
Differences in Heart rate variability before and after the laser irradiation compared to the sham group
Description
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.
Time Frame
Change from heart rate variability parameters at 67 days
Secondary Outcome Measure Information:
Title
Differences in the Epworth Sleepiness Scale (ESS) before and after the laser irradiation compared to the sham group.
Description
The Epworth Sleepiness Scale is widely used in the field of sleep medicine as a subje
Time Frame
Change from Baseline ESS at 67 days
Title
Differences in Visual Analogue Scale (VAS) before and after the laser irradiation compared to the sham group.
Description
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).
Time Frame
Change from Baseline VAS at 67 days
Title
Differences in scores of stroop test before and after the laser irradiation compared to the sham group.
Description
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.
Time Frame
Change from Baseline score of stroop at 67 days
Title
Differences in the Insomnia Severity Index (ISI) before and after the laser irradiation compared to the sham group.
Description
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.
Time Frame
Change from Baseline ISI at 67 days
Title
Differences in the Pittsburgh sleep quality index before and after the laser irradiation compared to the sham group.
Description
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.
Time Frame
Change from Baseline PSQI at 67 days
Title
Differences in The Beck Depression Inventory II (BDI-II) before and after the laser irradiation compared to the sham group.
Description
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.
Time Frame
Change from Baseline BDI-II at 67 days
Title
Differences in Beck Anxiety Inventory (BAI) before and after the laser irradiation compared to the sham group.
Description
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.
Time Frame
Change from Baseline BAI at 67 days
Title
Differences in Chinese 14-item PSS before and after the laser irradiation compared to the sham group.
Description
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.
Time Frame
Change from Baseline PSS at 67 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: 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. Exclusion Criteria: 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).
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Yuan-Pu Tseng, MD
Phone
886-2-28757453
Ext
230
Email
m061j3@gmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Yu-Ting Ho
Phone
886-968006520
Email
mascottofu@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Yuan-Pu Tseng, MD
Organizational Affiliation
Center for Traditional Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
Center for Traditional Medicine, Taipei Veterans General Hospital
City
Taipei
ZIP/Postal Code
112
Country
Taiwan
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Yuan-Pu Tseng, MD
Phone
886-2-28757453
Ext
230
Email
m061j3@gmail.com

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

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

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