Clinical Trial to assess efficacy of Parsana Acupressure Therapy plate in Type II Diabetes mellitus, Anxiety, Joint Pai
- Conditions
- Health Condition 1: F411- Generalized anxiety disorderHealth Condition 2: M255- Pain in jointHealth Condition 3: E119- Type 2 diabetes mellitus without complications
- Registration Number
- CTRI/2023/09/057271
- Lead Sponsor
- PARSANA Health Centre Pvt Ltd.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 47
Every Participants should fulfill the following eligibility criteria to
participate in the study:
1. Patients of either sex between the age 18 to 65 years.
2. Patients with Type II Diabetes mellitus, who are under Oral anti hyperglycemic drugs on a regular basis and whose random
blood glucose level is = 250mg/dl.
3. Type II Diabetic patients associated with Generalized Anxiety
Disorder and Joint Pain.
4. Patients who fulfill DSM IV and ICD-10 diagnostic criteria for
GAD will be included in the study.
5. Sustention of Chronic musculoskeletal pain due to
osteoarthritis, lower back pain, rheumatic arthritis, neck shoulder-arm syndrome, diabetic neuropathy for at least
minimum of 3 months or even more.
The following will be excluded from the study:
1. Uncontrolled Type II Diabetic mellitus though on Oral
anti-hyperglycemic drugs i.e., = 250mg/dl.
2. Patients with joint deformities.
3. Patients with co-morbid psychiatric disorders.
4. Patients with any other psychiatric diagnosis other than GAD.
5. Patients who are on regular treatment with psychotropic drugs at
least four weeks prior to the study.
6. Patients who are substance abuse like alcohol, drugs etc.,
7. Patients who are diagnosed with significant depression.
8. Patients with other complicated medical conditions as per the
investigator discretion are excluded from the study.
9. Pregnant or lactating females and women in childbearing age
refusing to use double barrier contraceptive methods.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method