The Effects of Self-Moxibustion Therapy on Subjective Physical Symptoms and Health-related Quality of Life of the Elderly. The Effects of Self-Moxibustion Therapy (moxa)

September 8, 2013 updated by: Jooshin Kim, Pusan National University

The Effects of Self-Moxibustion Therapy on Subjective Physical Symptoms and Health-related Quality of Life of the Elderly.

There will be significant differences between control and experimental group after the moxibustion intervention as to, subjective physical symptoms and quality of life.

Study Overview

Status

Completed

Intervention / Treatment

Study Type

Interventional

Enrollment (Actual)

70

Phase

  • Not Applicable

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

65 years to 85 years (Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Male and female older adults age between 65-85
  • Agree to participate and sign for the trail after understanding of study purpose, and method.
  • Able to answer for questions by verbally or literally
  • Able to participate in 2weeks after follow-up

Exclusion Criteria:

  • Having physical disorder such as thyroids, severe heart disease, dietetic mellitus, severe liver disease, allergy
  • Subjects who can not attend more than 3 times of intervention session
  • Subjects who are eligible by the decision of investigator

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: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: moxa
moxibustion treatment 3 times a week for 3 weeks
modernly developed moxibustion treatment device with safe cover on top of it.
Other Names:
  • Shinkigoo (신기구)
  • company: bosungsa

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
subjective physiological symptoms
Time Frame: 2 weeks after the intervention
2 weeks after the intervention

Secondary Outcome Measures

Outcome Measure
Time Frame
Quality of Life
Time Frame: 2 weeks after the intervention
2 weeks after the intervention

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Jooshin Kim, MSW, Pusan National University

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

April 1, 2013

Primary Completion (Actual)

May 1, 2013

Study Completion (Actual)

May 1, 2013

Study Registration Dates

First Submitted

March 2, 2013

First Submitted That Met QC Criteria

March 2, 2013

First Posted (Estimate)

March 5, 2013

Study Record Updates

Last Update Posted (Estimate)

September 10, 2013

Last Update Submitted That Met QC Criteria

September 8, 2013

Last Verified

September 1, 2013

More Information

Terms related to this study

Other Study ID Numbers

  • moxa201097603

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.

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