None listed
Conditions
Interventions
Visited once a week for a total of 12 weeks, with an exercise habit intervention based on foot-related information
Visited once a week for a total of 12 weeks, without an exercise habit intervention
Sponsors
Conditioning Lab Limited
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. male and female participants aged between 14 and 69 years at the time of obtaining consent through to the end of the study 2. individuals experiencing pain in the knee, lower back, or shoulder 3. individuals who have sufficient capacity to consent, have received a thorough explanation of the study's purpose and content, have fully understood it, and have voluntarily agreed to participate by signing a written consent form
Exclusion criteria
Exclusion criteria: 1.women who are pregnant (including those who may be pregnant) or currently breastfeeding 2.individuals who have been diagnosed with a disease related to the shoulder, lower back, knee, or foot within the past six months (those with pain but without a diagnosis are eligible to participate) 3.individuals whose NRS scores for the knee, lower back, and shoulder are all below 3, as reported in the questionnaire 4.women who are pregnant (including those who may be pregnant) or currently breastfeeding 5.individuals who have been diagnosed with a disease related to the shoulder, lower back, knee, or foot within the past six months (those with pain but without a diagnosis are eligible to participate) 6.individuals whose NRS scores for the knee, lower back, and shoulder are all below 3, as reported in the questionnaire 7.individuals with missing parts of the foot - such as toes or heel - that prevent full contact of the sole with the measurement device surface 8.individuals with allergies to any of the materials or components used in the devices or measurement instruments employed in this study 9.individuals who are unable to perform the full set of recommended exercises 10.individuals currently participating in another clinical study or who have participated in one within the past 4 weeks 11.individuals who, on the day of the examination, have injuries, dizziness, or other conditions that, in the judgment of the supervising physician, prevent them from safely maintaining a standing position or engaging in physical activity 12.any other individuals deemed unsuitable for participation by the study institution
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The Correlation Between Exercise Programs Suggested Based on Foot Information and Pain in the Knee, Lower Back, and Shoulder | — |
Countries
Japan
Contacts
Public ContactJunki Yamamura
Suntory Wellness Limited Service Promotion Department
Outcome results
None listed