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临床试验/NCT04516473
NCT04516473已完成不适用

The Impact of Abdominal Body Contouring Surgery on Physical Function After a Massive Weight Loss: a Non-randomized Control Trial

University of British Columbia1 个研究点 分布在 1 个国家目标入组 27 人开始时间: 2020年8月18日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
27
试验地点
1
主要终点
Change in physical function aggregate score

研究概览

简要总结

Obesity is a growing chronic medical condition in which as of 2015, a total of 107.7 million children and 603.7 million adults were considered obese and since 1980 the prevalence of obesity has doubled in more than 70 countries. It is estimated that 70 percent of individuals who undergo a massive weight loss would develop excess skin and based on patient reported outcome measures, it has been shown that excess skin negatively impacts patients' body image, self-esteem, physical function and body contouring surgeries have been demonstrated to improve these measures. These are surgeries that correct for excess skin and its adverse consequences. The form of the surgery is case dependent and can range from removing an apron of skin to complete contouring of the abdomen with tightening of the abdominal muscle and moving the belly button. Despite previous studies indicating mobility limitation because of excess skin and improvements after abdominal body contouring surgeries with the use of subjective measures of physical function, there are no studies that directly measures physical fitness post body contouring surgeries. Therefore, the purpose of the current study is to evaluate the impact of abdominal body contouring surgeries on direct objective measures of physical function.

It is hypothesized that 1) the removal of excess skin will improve direct objective measures of physical function in post massive weight loss participants 2) the removal of excess skin will improve direct measures of gait and balance in post massive weight loss participants 3) the removal of excess skin will improve patient reported outcome measures using quality of life questionnaires in post massive weight loss participants 4) the removal of excess skin will improve aerobic capacity in post massive weight loss participants 5) the removal of excess skin does not change the body composition in post massive weight loss participants.

详细描述

Participants will be recruited through multiple medical clinics and will visit the exercise, nutrition and muscle metabolism lab twice over the course of 8-12 weeks to complete objective and subjective measures of physical function. Each testing session will be conducted by the study investigator and physical function testing will be video recorded to reduce measurer bias. Based on participants' status they will be allocated to either a body contouring intervention group (BCI) or a post massive weight loss matched control (PMWMC). The first testing session would happen preoperatively and second one would happen between 8-12 weeks postoperatively depending on recovery required. Pain levels will be measured both pre and postoperatively using a numerical rating scale (0-10) to ensure adequate recovery.

Outcomes will include a variety of objective measures of physical function including 9-item modified physical performance test (mPPT), 30 second chair stand, timed up and go, stair climbing power, modified agility t-test, star excursion balance test, and 6 minute walk test. A body composition measure consisting of fat mass and fat free mass will also be obtained via dual-energy X-ray absorptiometry. Subjective measures would include 6 components of health related quality of life measure using BODY-Q questionnaire that would include sub scales such as body image, physical function, psychological, sexual, social, and obesity symptoms. Other subjective measure would include rate of perceived exertion which would be measured during each of the objective tests.

Additionally, grade of excess skin would be measured by images provided to the participants and weight of the resected excess skin will be obtained from the operating surgeon at the end of the study.

To obtain demographic history, physical activity level post surgery and to gain feedback for future clinical trial, the participants will also complete a socioeconomic status questionnaire, physical activity questionnaire, and participant experience with research questionnaire.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Prospective

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Weight has not deviated by greater than 5 percent for 3 months
  • Have excess grade skin of greater or equal to 2
  • Percent total weight loss pre-body contouring of greater or equal to 25 percent
  • Fluently read and write English

排除标准

  • Any musculoskeletal issues that would prevent participants from doing the physical function tests.
  • Current medication history indicating atypical antipsychotics including but not limited to clozapine, olanzapine, quetiapine, risperidone, aripiprazole, amisulpride, ziprasidone, asenapine, iloperidone, lurasidone and paliperidone.
  • Severe pulmonary conditions such as severe chronic obstructive pulmonary disease (COPD) and or severe asthma.
  • Participants who actively aiming to lose weight
  • Have diabetes with diabetic neuropathy or experienced hypoglycemic event within 6 months prior to the study
  • Severe kidney disease with estimated glomerular filtration rate (eGFR) less than 60 ml/min
  • Pregnant individuals
  • Uncontrolled hypertension with resting blood pressure greater than 160/90 mmHg
  • Uncontrolled obstructive sleep apnea with symptoms
  • On statin therapy with myopathy
  • Unstable atrial fibrillation
  • Weight pre-body contouring greater than 340 lbs (154 kg)
  • Current smoker

结局指标

主要结局

Change in physical function aggregate score

时间窗: 8-12 weeks

Measured by 9-item modified physical performance test that gives an aggregate score out 36 and comprises of 9 tests pre and post surgery and includes the following: 1. Time to complete a book lift 2. Time to complete putting on/off a lab coat 3. Time to complete picking up a penny from the floor 4. Time to complete a 5 times chair stand 5. Turning 360 degrees 6. Time to complete a 50 feet walk 7. Time to complete 1 flight of stairs 8. Completing 4 flights of stairs 9. A progressive romberg test Lowest score is 0, highest score is 36 and higher scores represent better outcomes.

次要结局

  • Change in lower body strength(8-12 weeks)
  • Change in dynamic balance balance(8-12 weeks)
  • Change in time to complete agility drill(8-12 weeks)
  • Change in timed up and go(8-12 weeks)
  • Change in aerobic capacity(8-12 weeks)
  • Change in rate of perceived exertion (RPE) during physical function tests(8-12 weeks)
  • Change in lean body mass(8-12 weeks)
  • Change in stair climbing power(8-12 weeks)
  • Change in fat mass(8-12 weeks)
  • Change in patient reported outcome measure of physical function and quality of life(8-12 weeks)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Cameron Mitchell

Assistant Professor

University of British Columbia

研究点 (1)

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