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Effects of Multisensory Home-based Programme on Psychological Well-being and Laboratory Outcomes among People with Metabolic Syndrome in Community

Phase 2
Recruiting
Conditions
Metabolic syndrome (MetS)
Metabolic syndrome, multisensory based programme, psychological well-being, occupational therapy
Registration Number
TCTR20240401007
Lead Sponsor
Faculty of Associated Medical Sciences, Chaing Mai University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
60
Inclusion Criteria

1. people who have three or more of the risk factors as defined by Harmonized criteria of MetS (Alberti et al., 2009), including elevated FPG at least 100 mg/dL or drug treatment of elevated glucose, elevated BP at least 130/85 mmHg or antihypertensive drug treatment, reduced HDL-C less than 40 mg/dL in male or 50 mg/dL in female or drug treatment for reduced HDL-C, elevated at least TG 150 mg/dL or drug treatment for elevated triglycerides, or WC at least 90 cm in male, at least 80 cm in female, 2. People who live in Nam Phrae sub-district, Hang Dong District, Chiang-Mai Province, 3. People with moderate to very high levels of stress as screened by using the Srithanya stress scale, 4. People who can communicate in the Thai language, 5. People who is willing to participate in this study and agree to sign an informed consent form

Exclusion Criteria

1. People who have been diagnosed with sensory impairment by a physician, 2.People who have been diagnosed with thyroid, respiratory, liver, kidney, or cardiovascular diseases by a physician, 3. People with history of serious mental illness, including depression, schizophrenia, bipolar disorder, anxiety disorder, and other psychotic disorders, 4. People with cognitive impairment, 5. People who receive drug treatment that will affect cortisol levels, including cushing drugs, antidepressant, antipsychotic, anti-anxiety, dopamine agents, opiod or antiopioids, drugs of abuse, hormones, rosiglitazone and pioglitazone

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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