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Effect of sprint exercise on depressio

Not Applicable
Conditions
Health Condition 1: null- Diagnosis of Depression will be according to DSM IV TR guidelines.
Registration Number
CTRI/2013/05/003625
Lead Sponsor
Deepmala Deore
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
40
Inclusion Criteria

presence of Depression According to DSM IV TR criteria. normal baseline ECG giving consent.

Exclusion Criteria

1.Resting blood pressure greater than or equal to 160/100 mm Hg

2.Factors that may limit adherence to intervention or affect conduct of the trial such as lack of time, amount of travel, and/or work or family stressors

3.Unable or willing to communicate with staff, to provide written informed consent, or accept the randomized assignment.

4.Failure to complete behavioral run-in and baseline testing

5.Not physically capable of performing the exercise required of the study protocols

6.Plans to be away in the next 6 weeks

7.Significant weight loss in the past year ( >20 kg) or current use of weight loss medications

8.Current diagnosis of schizophrenia, or other psychotic disorders, or bipolar disorder

9.History of bariatric surgery within last 3 years

10.Underlying diseases or conditions likely to limit lifespan and/or affect the safety of the intervention

11.Self-report HIV or tuberculosis

12.History or evidence of serious arrhythmias, cardiomyopathy, congestive heart failure, aortic aneurysm, or heart transplantation

13.Renal disease: currently receiving dialysis

14.Type I diabetes mellitus

15.Type 2 diabetes mellitus, defined as: Fasting plasma glucose levels greater than or equal to 126 mg/dL 2-hour postprandial Oral Glucose Tolerance Test results greater than or equal to 200 mg/dL.

16.Chronic obstructive lung disease, peripheral vascular disease, angina or any other disease that limits ability to follow exercise protocol

17.Advanced neuropathy or retinopathy.

18.Consuming alcoholic beverages, Smoker or have used nicotine/tobacco products within the last 12 months

Study & Design

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