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Signs and SymptomsSELHNCT01316029

Safety/Effectiveness Study of a Single Session of Laying-on-of-hands in Various Settings in Japan

An observational study of Signs and Symptoms and Physical Disorders, run by MOA Health Science Foundation at 1 site in Japan.

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

The purpose of this study is to determine the symptomatic changes after a single session of laying-on-of-hands in various settings, and to evaluate optimal conditions for the outcomes. Read more about this study

Who is it for?
Ages 16 years and olderHealthy volunteers can take part
What is being tested?
Okada Purifying Therapy
Type of treatment
Surgery or procedure
How many people
44,587 participants
Where
1 siteJapan
Study dates
Feb 2007to Dec 2007
Phase
Observational
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 16 years and older
  • All sexes
  • Healthy volunteers accepted
  • Child, Adult, Older adult

Study population: Any Japanese people who were interested in receiving laying-on-of-hands

Who may be able to join

  • able to receive laying-on-of-hands for 30 minutes or longer from the investigators
  • able to self-evaluate the change of their symptoms
  • competent to answer the Japanese questionnaires
  • aged 16 years or older

Who cannot join

  • those who did not match the inclusion criteria

Trial locations and contacts

1 site in 1 country.

Japan1 site
  • MOA Health Science Foundation

    Tokyo, Tokyo, 108-0074

Other trials in Japan

About this study

Official title: A Large Cross-sectional Study of Laying-on-of-hands in Japan: Who Responds to it and What Facilitates the Response?

The purpose of this study is to determine the symptomatic changes after a single session of laying-on-of-hands in various settings, and to evaluate optimal conditions for the outcomes.

Read the detailed description

Laying-on-of-hands is applied in many different situations; however, most reports published previously described its efficacy in a clinical setting, with its administration conducted by a few expert practitioners. This study aimed to determine the symptomatic changes after a single session of the Okada Purifying Therapy, a form of laying-on-of-hands, in various settings, and to analyze factors influencing the outcomes.

Being tested
Okada Purifying Therapy
Keywords
Laying-on-of-hands, Therapeutic touch, cross-sectional study, healing environment, safety and effectiveness, optimal condition for the intervention
Medical subject headings
Signs and Symptoms, Personal Satisfaction

What participants receive

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

  • Okada Purifying TherapyProcedure or surgery

    Also called laying-on-of-hands, biofield therapy, Therapeutic touch

    Each participant received a single session of Okada Purifying Therapy lasting 30 minutes or longer, administered by a voluntary certified practitioner.

Study groups in NCT01316029
Study groupRoleWhat they receive
laying-on-of-hands44,587 Japanese volunteers with/without illness, who were interested in receiving laying-on-of-hands
Receives: Procedure: Okada Purifying Therapy

What is being measured

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

  1. Severity of various symptoms

    Participants self-evaluated the severity of various symptoms before and after the intervention, and determined whether their symptoms got better, worsened, or did not change.

    Measured: Baseline and immediately after a single intervention

Secondary outcomes (1)
  1. Adjusted odds ratios of the factors influencing the outcomes

    After collecting all the eligible data, to be clarified are such personal variables as demographic attributes associated with the tendency to respond, and factors that facilitate such responses.

    Measured: in 1 year

Timeline

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

  1. First posted16 Mar 2011 (estimated)
  2. Study startFeb 2007
  3. Primary completionDec 2007
  4. Study completionDec 2007

Resources

More details

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

Study design
Study type
Observational
Observational model
Ecologic or community
Time perspective
Cross-sectional
Enrolment
44,587 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01316029
Sponsor's protocol ID
MHS-001
Acronym
SELH
Status last verified
Jan 2007
First submitted
15 Mar 2011
Last updated
16 Mar 2011
Results posted
No
Data monitoring committee
No

Questions about this trial

What is this clinical trial studying?

An observational study of Signs and Symptoms and Physical Disorders, run by MOA Health Science Foundation at 1 site in Japan.

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 4 inclusion and 1 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 16 Mar 2011. 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 Japan. 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?

Severity of various symptoms (time frame: Baseline and immediately after a single intervention). 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 16 Mar 2011.

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