Clinical Trials Directory

Trials / Terminated

TerminatedNCT00911209

Weight Loss in Pre-Hypertensive Patients With Diastolic Dysfunction

Impact of Weight Loss on Diastolic Dysfunction in Overweight Pre-Hypertensives

Status
Terminated
Phase
N/A
Study type
Interventional
Enrollment
1 (actual)
Sponsor
Ragavendra Baliga · Academic / Other
Sex
All
Age
21 Years
Healthy volunteers
Not accepted

Summary

The focus of this study is to observe the impact of weight loss in overweight individuals who have pre-hypertension (have a blood pressure reading of 121-139/81-89 mm Hg). The specific focus is to observe the difference in diastolic dysfunction (heart function) in these individuals at the beginning of the study and then again after 24-28 weeks. Diastolic dysfunction in this population indicates an increased risk of heart failure in the future. The aim of this study is to prevent or reduce the risk of heart failure in overweight individuals with pre-hypertension.

Detailed description

You will be enrolled in the study for 24-28 weeks and will be randomly assigned to one of two assigned group. One group of subjects (Intervention group) will receive information on Heart healthy diet, lifestyle recommendations and diet and exercise counseling with a dietitian in order to achieve at least 7% weight loss. The other group will receive standard of care i.e., Information on Heart healthy diet at baseline visit (Standard of care group). The following is the time line of activities anticipated by the subject in each group. Both the groups will be screened at 3 different visits within 4 weeks to determine eligibility. If you are eligible they will be randomized to either be in Standard of care group or Intervention group. After randomization, the "Standard of care group" will come for Baseline and Final visit (24th week). The Intervention group will have 14 weekly visits with a nutritionist and 1 monthly visit, about 40-50 minutes each visit (total of 15) in 24- 28 week time frame. The second monthly session will be the final assessment visit. Both the groups will have a Baseline Assessment and a Final Assessment visit which will last about 3 hours.

Conditions

Interventions

TypeNameDescription
BEHAVIORALDietitian counsellingOnce a week for 14 weeks then 1 monthly visit. Visits last 40-50 minutes

Timeline

Start date
2008-07-01
Primary completion
2010-12-01
Completion
2010-12-01
First posted
2009-06-01
Last updated
2012-10-15

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00911209. Inclusion in this directory is not an endorsement.

Weight Loss in Pre-Hypertensive Patients With Diastolic Dysfunction (NCT00911209) · Clinical Trials Directory