Efficacy of a Web-based Lifestyle Modification Program in Obese Patients With Cardiovascular Risk Factors

Obesity Clinical Trial

Official title:

A 6-Month, Randomized Study to Evaluate the Efficacy of a Web-based Lifestyle Modification Program With and Without Telephone Counseling Support

Clinical Trial Details — Status: Withdrawn

Administrative data

• NCT number: NCT01664026
• Other study ID #: PWeb123
• Status: Withdrawn
• Phase: N/A
• Start date: August 2012
• Est. completion date: December 2013

Study information

• Verified date: January 2019
• Source: Clínica Bazterrica
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

To evaluate the effect of a 6-month web-based lifestyle modification program with and without telephone counseling versus usual care in obese patients with cardiovascular risk factors on:

• Weight Loss

• Waist circumference; blood pressure; total cholesterol, triglycerides, LDL-cholesterol, HDL-cholesterol; glucose and hemoglobin A1c; C-reactive protein.

• Physical activity and eating habits

• Quality of life

Recruitment information / eligibility

• Status: Withdrawn
• Enrollment: 0
• Est. completion date: December 2013
• Est. primary completion date: August 2013
• Accepts healthy volunteers: No
• Gender: All
• Age group: 25 Years to 70 Years

Eligibility

Inclusion Criteria:

1. Male or female 25-70 years of age

2. Obese (BMI = 30 kg/m2 and <40 kg/m2)

3. At least 2 cardiovascular risk factors (diabetes, hypertension or dyslipidemia) i) Hypertension defined by a history of hypertension, treatment of hypertension or BP values >140/90 mmHg in two consecutive office visits ii) High cholesterol defined by an LDL-C =130 mg/dL and/or HDL-C <40 mg/dL and triglycerides =150 mg/dL iii) Type 2 Diabetes Mellitus defined by a history of diabetes, treatment of diabetes or fasting glucose =126 mg/dL in two consecutive office visits

4. Participant must be willing and able to provide written informed consent

5. Participant must be willing and able to comply with study related procedures

6. Participant must have access to Internet and e-mail

Exclusion Criteria:

1. Stage 1 or 2 on Patient Activation Measures tool

2. Weight change of more than 5 kg during the 3 months preceding the screening visit

3. History of bariatric surgery

4. Fasting Plasma Glucose at screening > 250 mg/dL (> 13.9 mmol/L)

5. Hemoglobin A1c at screening >8.5%

6. Treatment of type 2 diabetes with insulin (except for history of intermittent acute use, no more than 2 weeks usage in previous 6 months)

7. Uncontrolled or inadequately controlled hypertension at the time of screening with blood pressure >160/100 mmHg

8. Secondary hypertension

9. Changes in lipid, blood pressure or diabetes modifying agents including introduction, change in dose or cessation in the 3 months prior to Screening Visit

10. Personal history of coronary heart disease, congestive heart failure, serious arrhythmias and stroke

11. Cardiovascular, hepatic, neurological, endocrine disease, active malignant tumor or other major systemic disease making implementation of the protocol or interpretation of the study results difficult.

12. Presence of any condition (medical, psychological, social, or geographical), actual or anticipated, that in the opinion of the Investigator would restrict or limit the patient's successful participation for the duration of the study

13. Presence of history of cancer within the past five years with the exception of adequately treated localized basal cell skin cancer or in situ uterine cervical cancer

14. Use of systemic glucocorticoids (excluding topical application or inhaled forms) for one week or more within 3 months prior to the time of screening

15. Use of any investigational agent (drug, biologic, device) within 3 months prior to screening

Related Conditions & MeSH terms

• Obesity

Intervention

Behavioral:
• Web-based lifestyle modification
Access to a web-based lifestyle modification program of 6-month duration that covers all aspects of a healthy lifestyle including physical activity, nutrition and weight maintenance.
• Web-based lifestyle modification +
Access to a web-based lifestyle modification program of 6-month duration that covers all aspects of a healthy lifestyle including physical activity, nutrition and weight maintenance plus telephone counseling support by health coaches on a weekly or bi-weekly basis.

Locations

Country	Name	City	State
Argentina	Clinica Bazterrica	Buenos Aires

Sponsors (1)

Lead Sponsor	Collaborator
Clínica Bazterrica

Country where clinical trial is conducted

Argentina, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Changes in lifestyle behaviors (physical activity and eating habits)		6 months
Other	Changes in quality of life		6 months
Primary	Change in body weight from randomization to 6 months		6 months
Secondary	Changes in waist circumference		6 months
Secondary	Changes in blood pressure		6 months
Secondary	Changes in lipid parameters (total cholesterol, triglycerides, LDL-cholesterol, HDL-cholesterol)		6 months
Secondary	Changes in glycemic parameters (glucose and hemoglobin A1c)		6 months
Secondary	Changes in C-reactive protein		6 months