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HospiceNCT03939221

Measure the Meridian Energy Change of Terminal Hospice Patient Via Meridian Energy Analysis Device

A study testing Infrared Lamp and Acupressure in people with Hospice and Survival, run by Changhua Christian Hospital at 1 site in Taiwan.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

In the hospice ward, there are lots of suffered hospital patients with multiple physical discomfort related to terminal disease. Investigators want to use an objective measure instrument to monitor the effects of complementary and alternative medicine and clinical symptoms. Read more about this study

Who is it for?
Ages 20 to 99 years
Conditions the study is for
Hospice, Survival, Alternative Medicine
What is being tested?
Infrared Lamp and Acupressure
Could I receive a placebo?
No, everyone receives an active treatment
How many people
200 participants
Where
1 siteTaiwan
Study dates
18 Feb 2019to 30 Oct 2020
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 99 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Patients lived at our Changhua Christian Hospital hospice ward
  • From 2019-02~2020-12, age 20 to 99 years old, volunteer patient

Who cannot join

  • Unwillingness
  • Wound or amputation near wrist or ankle
  • Severe agitation or seizure patients

Trial locations and contacts

1 site in 1 country.

Taiwan1 site
  • Changhua Christian Hospital

    Changhua, 500

Other trials in Taiwan

About this study

Official title: Measure the Meridian Energy Change of Terminal Hospice Patient Via Meridian Energy Analysis Device to Evaluated the Relationship of Clinical Symptoms and Alternative Medicine Effect.

In the hospice ward, there are lots of suffered hospital patients with multiple physical discomfort related to terminal disease. Investigators want to use an objective measure instrument to monitor the effects of complementary and alternative medicine and clinical symptoms. First, investigators use the Meridian Energy Analysis Device (MEAD) to measure the bilateral 12 Yuan points (primary points) of terminal hospice patients. It provides the prediction value between terminal disease and the change of different meridian energy. Besides, the meridian energy value maybe predict the survival period. Then, the intervention of complementary and alternative medicine can also monitor via MEAD.

Read the detailed description

In the hospice ward, there are lots of suffered hospital patients with multiple physical discomfort related to terminal disease. It may be caused by cancer or multiple kinds of organ failure. The terminal hospital patients have symptoms such as pain, dyspnea, fatigue, nausea, vomiting, poor appetite, constipation, ileus or edema…, etc. Investigators want to use an objective measure instrument to monitor the effects of complementary and alternative medicine.

First, investigators use the Meridian Energy Analysis Device (MEAD) to measure the bilateral 12 Yuan points (primary points) of terminal hospice patients (divided to cancer, multiple kinds of organ failure). It provides the prediction value between terminal disease and the change of different meridian energy. Besides, the meridian energy value maybe predict the survival period. Then, investigators use the intervention of complementary and alternative medicine (like infrared lamp and acupressure…, etc.) to improve the quality of life in the terminal hospice patients. Also, investigators will use the Meridian Energy Analysis Device, pain scale, vital signs and quality of life scale (SF-36) to evaluate the effects of complementary and alternative medicine.

Being tested
Infrared Lamp and Acupressure
Keywords
skin electric conductance, survival period, complementary and alternative medicine

What participants receive

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

  • Infrared Lamp and AcupressureBehavioural

    Measure the ankle and wrist acupoints skin conductance to evaluate the basic condition of terminal hospice patients. Then investigators use the infrared lamp and acupressure(tender points, PC6 and ST36 for one minutes) for our patient for the cold limbs, pain control and constipation problems.

Study groups in NCT03939221
Study groupRoleWhat they receive
intervention of infrared lamp and acupressureExperimentalMeasure the ankle and wrist acupoints skin conductance to evaluate the basic condition of terminal hospice patients. Then investigators use the infrared lamp and acupressure(tender points, PC6(neiguan) and ST36(zusanli) for one minutes) for our patient for the cold limbs, pain control and constipation problems.
Receives: Behavioral: Infrared Lamp and Acupressure

What is being measured

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

  1. The change of 24 points skin electric conductance over bilateral wrist and foot in terminal patients

    Investigators use the meridian energy analysis device to measure the 24 points skin conductance over bilateral wrist and foot. The meridian energy analysis device is an electrophysiology tool to measure the skin micro-electrical currents(range from 0uA to 200uA). The higher skin conductance stands for better condition of patient. Investigators will evaluate the relationship between the skin conductances and clinical symptoms. Then investigators will check the effect via the skin electric conductance before and after the infrared lamp and acupressure intervention.

    Measured: through hospitalization period, an average of 1 month (after admission baseline evaluation and till discharge)

Timeline

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

  1. First posted6 May 2019
  2. Study start18 Feb 2019
  3. Primary completion30 Oct 2020
  4. Study completion30 Oct 2020

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
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
200 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03939221
Sponsor's protocol ID
CCH-181018
Status last verified
Jan 2019
First submitted
7 Apr 2019
Last updated
24 Aug 2021
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing Infrared Lamp and Acupressure in people with Hospice and Survival, run by Changhua Christian Hospital 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 2 inclusion and 3 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: finished, as of the sponsor's last update on 24 Aug 2021. 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. 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?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

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

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

The change of 24 points skin electric conductance over bilateral wrist and foot in terminal patients (time frame: through hospitalization period, an average of 1 month (after admission baseline evaluation and till discharge)). 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 24 Aug 2021.

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