Community-Based Detection and Treatment of Peripheral Arterial Disease in Hispanics.

Not Applicable

Completed

Conditions: Peripheral Arterial Disease

Interventions: Other: Supervised exercise Program

Registration Number: NCT01440634

Lead Sponsor: University of Texas Southwestern Medical Center

Brief Summary: Peripheral Arterial Disease (PAD) is a highly prevalent public health problem that results from progressive atherosclerosis of arteries in the lower extremities. PAD is also associated with major detrimental effects on quality of life and functional status, and is the most important cause of limb amputation. More importantly, PAD is a major manifestation of cardiovascular disease and a potent predictor of myocardial infarction, stroke and death. Despite its frequent occurrence, little is known about the natural history of PAD in Hispanics who represent 12.5% of the United States. Because access to health care is limited among Hispanics, CBPR is the ideal process to reach this target population. The goal of the proposed study is to evaluate community-based strategies of detection and treatment of peripheral arterial disease (PAD) in Hispanics. The proposed project consists of two phases: a cross-sectional phase (PAD detection), followed by a randomization phase.During the PAD detection study , the prevalence and severity of PAD in this population will be determined. Specific risk factors associated with PAD among the Hispanic participants will be identified. During the second phase patients will be enrolled in a randomized, non-blinded trial comparing a community-based risk factor modification and supervised exercise program versus usual care for PAD. These individuals will undergo a baseline evaluation similar to the one obtained during the first phase of the study, but will also include functional testing of the lower extremities.

Detailed Description: Not available

Recruitment & Eligibility

Status: COMPLETED

Sex: All

Target Recruitment: 347

Inclusion Criteria

Cross-Sectional phase:

Hispanic men and women aged 70 years or older.
Hispanic participants with diabetes mellitus or smokers aged 50 through 69 years.
Individual has been informed of the nature, procedures and risks of the study, and has signed a consent form approved by UT Southwestern Institutional Review Board.

Randomization phase:

Hispanic men and women aged 70 years or older
English or Spanish speaking
Hispanic participants with diabetes mellitus or smokers aged 50 through 69 years.
Documented peripheral arterial disease with an Ankle-brachial index (ABI) < 0.9 or Toe-brachial index (TBI) <0.7, and abnormal Pulse Volume Recordings (PVR).
Ability to ambulate independently.
No prior amputations other than toe or partial foot amputations that do not impede walking.
Patient has been informed of the nature, procedures and risks of the study, and has signed a consent form approved by the UT Southwestern Institutional Review Board.

Exclusion Criteria

Cross-Sectional Phase

Individuals with severe dementia.
Individuals with inability to provide informed consent.
Bilateral lower or upper extremities amputations.
Pregnancy or lactation. Randomization Phase
Non-ambulatory
Individuals with prior below- or above-knee amputations
Individuals unable to give informed consent
Individuals unwilling to perform the functional tests or quality of life assessments
Individuals unable to perform exercise therapy, functional tests or quality of life assessments due to severe comorbidities
Presence of concurrent illness with an anticipated life expectancy less than six months
Individuals with planned operative interventions

Study & Design

Study Type: INTERVENTIONAL

Study Design: CROSSOVER

Arm && Interventions

Group	Intervention	Description
supervised exercise	Supervised exercise Program	It consists of six months of supervised, intermittent track walking to near maximal leg pain or discomfort three days per week. Walking duration will begin at 20 - 30 minutes per session for the first month of the program, and increased by 5 minutes per session per month until a total of 45 minutes of walking per session is reached by the third month.

Primary Outcome Measures

Name	Time	Method
Effect of an Exercise Intervention on Walking Ability (Functional Outcome)	6 months	Walking distance (Six-Minute Walk test). Following a standardized protocol, individuals are instructed to walk back and forth a 100-ft hallway as far as they can in six minutes after instructions to cover as much distance as possible. A research assistant walks slightly behind each participant so as not to pace the individual. The research assistant records whether or not each person stops during the 6-minute walk. During the proposed study, members of the research team and trained lay health promoters (LHPs) will walk directly behind the individuals and give standardized instructions of encouragement at set intervals. Data will be reported on meters walked.

Secondary Outcome Measures