MedPath

Examination of improvement of constipation by Tanden breathing

Phase 2
Conditions
constipations
Registration Number
JPRN-UMIN000035662
Lead Sponsor
Okayama University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
21
Inclusion Criteria

Not provided

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

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
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 Outcome Measures
NameTimeMethod
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
© Copyright 2025. All Rights Reserved by MedPath