Investigation for Health Efficacy of Infrared-C Radiation on Diabetes Patients in Senior's Activity Center

November 22, 2019 updated by: Nanhua University
Hyperglycemia caused by diabetes will bring us the long-term damage,it causes glycation. The combination of sugar molecules and protein molecules will transform to advanced glycation end products (AGEs) and produce a lot of free radicals to caused inflammatory reactions, forming various comorbidities, affecting the function of different organs, especially the eyes, kidneys, nervous system, heart, blood vessels and damage to bone structure and bone Quality, which leads to bone loss. Therefore, the development of alternative therapies is important for the treatment of diabetes. We assume the 4 months experiment can normalize subjects HbA1c.

Study Overview

Detailed Description

In the past research from our team, it was found that far infrared ray (FIR) helps to reduce oxidative stress in the body and is expected to contribute to the treatment of diabetes. Therefore, the team hopes to effectively reduce glycated hemoglobin (HbA1c), fasting blood glucose (GLU-AC), insulin (insulin), reduce the body's oxidative stress index, increase Total Antioxidant Capacity (TAC) inhibit the inflammatory response and reduce complications through 4 months of IR-C intervention. Which expected to reduce the index of the nitrogen-type first collagen element (Procollagen-I N -telopeptide, PINP) and C-telopeptide of type I collagen (CTx) bone loss index, enhance Osteocalcin's index of bone growth indicators. Along with the Pittsburgh sleep quality index (PSQI), numeric rating scale-knee (NRS-knee) and Geriatric depression Scale-15 (GDS-15) to reduce the number of times the elderly take medication and improve their health and quality of life.

Study Type

Interventional

Enrollment (Anticipated)

64

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Chiayi
      • Dalin, Chiayi, Taiwan, 62249
        • Recruiting
        • Department of Natural Biotechnology, Master's program in Natural Healing Sciences Nanhua University
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

50 years to 85 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • HbA1c higher than 6.8% or fasting blood sugar higher than 126mg/dL;
  • Conscious, mental and cognitively normal;
  • no obstacles in action;
  • can read, write and communicate with mandarin, taiwanese and hakka.

Exclusion Criteria:

  • Inflammatory skin wounds on the neck, back, lower back or lower leg;
  • obstacles in communication;
  • People with disabilities, epilepsy, and other unacceptable warming treatments;
  • When the subject finds that he or she is unwell during the procedure, the experiment is terminated and take care by the medical staff.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Supportive Care
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Experiment Group
lay on the FIR-C mattress with cover the FIR-C abdominal pad on abdominal part and Knee part during the sleeping time. The controller will switch on and switch off rotated in each hour for whole night.
infrared-C irradiation by hot mattress with a powered heating compress
infrared-C irradiation by hot abdominal pad with a powered heating compress
Placebo Comparator: Control Group
lay on the FIR-C mattress with cover the FIR-C abdominal pad on abdominal part and Knee part during the sleeping time. The controller will switch on and switch off rotated in each hour for whole night. the FIR-C mattress and the FIR-C abdominal pad is malfunction and it can not produce the FIR-C.
normal mattress with fake controller, custom make for placebo group
normal abdominal pad with fake controller, custom make for placebo group

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Hemoglobin A1c, HbA1c
Time Frame: Baseline to 4 months
The hemoglobin A1c can show us our average level of blood sugar over the past 2 to 3 months. Below 6% is normal, over 6% is abnormal.
Baseline to 4 months
Fasting Blood Sugar, GLU-AC
Time Frame: Baseline to 4 months
A blood sample will be taken after an overnight fast which to estimate blood sugar levels. Below 100mg/dL is normal, 100 to 125mg/dL is prediabetes, 125mg/dL above is consider diabetes.
Baseline to 4 months
Insulin
Time Frame: Baseline to 4 months
Is a hormone that is produced and stored in the beta cells of the pancreas. this test can measures the amount of insulin in the blood which to analyze the insulin resistance of the body.
Baseline to 4 months
Superoxide, O2-
Time Frame: Baseline to 4 months
superoxide is one type of the free radical. The assay of superoxide can show us the ability to inhibit free radical contained in blood. The highest value of it means the highest injured did. The data of the post-test should be lower than the data of the pre-test.
Baseline to 4 months
Osteocalcin
Time Frame: Baseline to 4 months
Is a noncollagenous protein hormone found in bone and dentin, it implicated in bone mineralization and calcium ion homeostasis. The normal range for female: 12-23ng/dL; the normal range for male: 17-26ng/dL.
Baseline to 4 months
Procollagen-I N-telopeptide, PINP
Time Frame: Baseline to 4 months
This market is a specific indicator of type I collagen deposition therefore can set as an indicator of bone formation velocity. The reference's range for PINP: 16.27 - 73.87 ng/mL.
Baseline to 4 months
C-telopeptide of type I collagen,CTx
Time Frame: Baseline to 4 months
It is the carbon-terminal fragment of the first type of collagen in the bone, which is the final product of bone decomposition and can be used as an indicator of bone loss. The reference's range for female: 0.104-1.008ng/mL; for male: 0.000-0.854ng/mL
Baseline to 4 months
Total Antioxidant Capacity, TAC
Time Frame: Baseline to 4 months
to assess the antioxidant status of blood to evaluate the antioxidant response against the free radicals produced in the blood. The reference's range for male: >=0.65mmol/L; female: >=0.54mmol/L
Baseline to 4 months
Advanced glycation end-product,AGEs
Time Frame: Baseline to 4 months
AGEs are proteins or lipids that become glycated as a result of exposure to sugars. Its can be a factor in aging and in the development from diabetes. The highest value of it means the highest injured did. The data of the post-test should be lower than the data of the pre-test.
Baseline to 4 months
Insulin resistance assessment
Time Frame: Baseline to 4 months
to measure the insulin sensitivity of the cells, the Homeostasis Model Assessment for Insulin Resistance (HOMA-IR) method will be applied in this study. The highest value of it means the highest injured did. The data of the post-test should be lower than the data of the pre-test.
Baseline to 4 months
Beta-cell function assessment
Time Frame: Baseline to 4 months
to measure the function of the Beta-cell, the HOMA-beta-cell method will be applied in this study. The highest value of it means the function of the Beta-cell more normal. The data of the post-test should be higher than the data of the pre-test.
Baseline to 4 months
Autonomic nervous system assessment - Heart Rate
Time Frame: Baseline to 4 months

the measurement of Autonomic nervous system assessment is to measure the functions of sympathetic and the parasympathetic. The scale of this assessment is HR(Heart Rate).

HR(1/min):normal range(60-100),abnormal range(lower than 60 or higher than 100)

Baseline to 4 months
Autonomic nervous system assessment - blood pressure
Time Frame: Baseline to 4 months

the measurement of Autonomic nervous system assessment is to measure the functions of sympathetic and the parasympathetic. The scale of this assessment is about blood pressure.

SYS(mmHg):normal range(90-140), abnormal range(higher than 140) DIA(mmHg):normal range(60-90), abnormal range(higher than 90) SYS(mmHg) and DIA(mmHg) will be combined to report blood pressure in SYS/DIA(mmHg)

Baseline to 4 months
Autonomic nervous system assessment - Heart Rate Variability
Time Frame: Baseline to 4 months

the measurement of Autonomic nervous system assessment is to measure the functions of sympathetic and the parasympathetic. The scale of this assessment is about HRV(Heart Rate Variability).

HRV(ms): normal range(25-100), abnormal range(lower than 15)

Baseline to 4 months
Autonomic nervous system assessment - Low Frequency
Time Frame: Baseline to 4 months

the measurement of Autonomic nervous system assessment is to measure the functions of sympathetic and the parasympathetic. The scale of this assessment is about LF(Low Frequency %).

LF(%): normal range(40-70), abnormal range(higher than 80)

Baseline to 4 months
Autonomic nervous system assessment - High Frequency
Time Frame: Baseline to 4 months

the measurement of Autonomic nervous system assessment is to measure the functions of sympathetic and the parasympathetic. The scale of this assessment is about HF(High Frequency %).

HF(%): normal range(25-40), abnormal range(lower than 20)

Baseline to 4 months
Autonomic nervous system assessment - Low/High Frequency standard
Time Frame: Baseline to 4 months

the measurement of Autonomic nervous system assessment is to measure the functions of sympathetic and the parasympathetic. The scale of this assessment is about LF/HF(Low/High Frequency standard).

LF/HF: normal range(0.5-2.5), abnormal range(higher than 3)

Baseline to 4 months
Autonomic nervous system assessment - Irregular Heartbeat standard
Time Frame: Baseline to 4 months

the measurement of Autonomic nervous system assessment is to measure the functions of sympathetic and the parasympathetic. The scale of this assessment is about IR(Irregular Heartbeat standard).

IR: normal range(0-3), abnormal range(higher than 4)

Baseline to 4 months
Pittsburgh sleep quality index (PSQI)
Time Frame: Baseline to 4 months
The PSQI is a questionnaire to measure sleep quality over the past month. the 19 items question can be grouped into 7 components, its (1)sleep duration; (2) sleep disturbance;(3) sleep latency; (4) daytime dysfunction due to sleepiness; (5) sleep efficiency; (6) overall sleep quality; (7) sleep medication use. The sleep component scores are summed to a total score ranging from 0 to 21. The higher of the total score means the sleep quality worse.
Baseline to 4 months
Knee Pain - Numeric Rating Scale, Knee Pain - NRS
Time Frame: Baseline to 4 months
To measure the Knee's painfulness. The higher of the score means the knee's more painful.
Baseline to 4 months
Geriatric Depression Scale-15, GDS-15
Time Frame: Baseline to 4 months

to assess depressive symptoms among old people with differing level of cognitive function.

1-5 : healthy 6-9 : light depression 10 and above : serious depression

Baseline to 4 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Ching Yong Chin, Master, Nanhua University
  • Principal Investigator: Yi-Wen Huang, Master, Nanhua University
  • Principal Investigator: Jin-Bang Shang, Master, Nanhua University

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

March 23, 2018

Primary Completion (Anticipated)

December 31, 2019

Study Completion (Anticipated)

February 15, 2020

Study Registration Dates

First Submitted

June 8, 2019

First Submitted That Met QC Criteria

November 22, 2019

First Posted (Actual)

November 26, 2019

Study Record Updates

Last Update Posted (Actual)

November 26, 2019

Last Update Submitted That Met QC Criteria

November 22, 2019

Last Verified

November 1, 2019

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Diabetes Mellitus, Type 2

Clinical Trials on FIR-C mattress

Subscribe