Progressive Resistance Training in Patients With Class III Obesity

Beth Israel Lahey Health

Status: Completed

Conditions: Obesity

Treatments: Behavioral: Progressive Resistance Training

Study type: Interventional

Funder types: Other

Identifiers

NCT01100450

2009P000083

Details and patient eligibility

About

To test the strength and physical performance outcomes of a 12-week progressive resistance training (PRT) exercise program in a small cohort of patients with Class III obesity who are preparing for bariatric weight loss surgery at Beth Israel Deaconess. The study will also test patient compliance to the 12 week PRT program. Whereas PRT exercise is currently recommended as a part of preoperative clinical care for bariatric surgery patients, little research has been done to measure the acceptance and effectiveness of a standardized PRT exercise protocol for improving health and perioperative care. Preliminary data from this study could be used to justify larger studies and further investigation.

Enrollment: 6 patients

Sex: All

Ages: 18 to 65 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Men and women 18-65 years old

• A BMI of ≥40 kg/m2

• Considering Weight Loss Surgery at BIDMC

• Participating in multidisciplinary preoperative program:

  • been determined by a mental health professional (i.e., psychologist or social worker) to be well-informed, motivated, and not symptomatic for psychopathology that would put the person at risk for injury or failure with WLS
  • expressed strong desire for significant weight loss
  • experienced documented failure of long-term weight loss using nonsurgical methods
  • been informed of and accepts risks of surgery

• Cleared by their primary care physician to be in stable health and capable of moderate level exercise

• Willing to comply with expected attendance and participation at all intervention sessions and testing appointments

• Has reliable transportation to the intervention location

Exclusion criteria

• Orthopedic limitations that would preclude exercise testing and training

Trial design

Primary purpose: Health Services Research

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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6 participants in 1 patient group

Resistance Training

Experimental group

Treatment:

Behavioral: Progressive Resistance Training