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Examination of improvement of constipation by Tanden breathing

Examination of improvement of constipation by Tanden breathing - Examination of improvement of constipation by Tanden breathing

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000035662
Enrollment
40
Registered
2019-01-25
Start date
2019-02-18
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

constipations

Interventions

Stratified randomized weight list comparison test Intervention group 6 week intervention (daily Tanden breathing for about 10 minutes) Wsiting group 6 weeks waiting - 6 week intervention (daily

Sponsors

Okayama University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Those who are conscious of constipation symptoms during the past month of acquiring consent. Japanese version Constipation Assessment scale CAS Ver.2 - MT Person who has 5 points or more in MT with a score of 5 or more. After receiving sufficient explanation for participation in this research, those who gained document consent by their own free will with sufficient understanding.

Exclusion criteria

Exclusion criteria: 1.A woman who is pregnant or has a possibility of pregnancy 2.Persons who already have custom of Tanden breathing. (Excluding those who have experience, but who are not customary.) 3.Other persons who have judged that the researcher or research cooperator is inappropriate as the research subject

Design outcomes

Primary

MeasureTime frame
The score of the Japanese version of constipation assessment scale at each timing is defined as follows. S 12 = 6 weeks after intervention group intervention (intervention group) S10 = baseline measurement (intervention group) S02 = 6 weeks after intervention group intervention (waiting group) S00 = Baseline measurement (waiting group) Primary out comes are E {(S12 - S10) - (S02 - S00)}. Note that E (x) indicates the expected value of x.

Secondary

MeasureTime frame
S 04 = 6 weeks after waiting group intervention (waiting group) S 11 = 3 weeks after intervention group intervention (intervention group) S 03 = 3 weeks after waiting group intervention(waiting group) S01 = 3 weeks after intervention group intervention (waiting group) Perform comparison within the county in the waiting group. E (S 04 - S 02) is calculated. Calculate intra-county comparison E (S 11 - S 10) and E (S 12 - S 11) in the intervention group. Calculate intra-county comparison E (S 03 - S 02) and E (S 04 - S 03) in the waiting group. Inter-group comparison E {(S 11 - S 10) - (S 01 - S 00)} is calculated. Subjective symptoms

Countries

Japan

Contacts

Public ContactHiroshi Habu

Okayama University Graduate School of Medicine,Dentistry and Pharmaceutical Sciense Department of Epidemiology

p17z9kt4@s.okayama-u.ac.jp086-235-7173

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026