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临床试验/NCT04014296
NCT04014296已完成不适用

Effects of Dietary Protein Intake and Resistance Training on Retention of Fat Free Mass During Weight Loss in Adults Over 50 with Obesity

University of Alabama at Birmingham2 个研究点 分布在 1 个国家目标入组 89 人开始时间: 2021年4月12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
89
试验地点
2
主要终点
Class Attendance

研究概览

简要总结

The purpose of this study is to examine the separate and combined effects of a high-protein (HP) diet and resistance training (RT) on body composition and potential biological moderators of body weight in women and men >50y. All participants will receive dietary physical activity guidance through our group-based weight loss program, State of Slim (SOS). The SOS program will be delivered via the Zoom videoconferencing platform. These participants will be randomized to receive either a counseling-based HP diet plan or RT plan. Body composition assessments at 8 wk will identify responders and non-responders; the latter will be re-randomized to "augment" (HP: add protein supplements; RT: supervise RT) or "combine" (HP with protein supplements + supervised RT).

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Sequential
主要目的
Other
盲法
None

入排标准

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

入选标准

  • Male or Female
  • Age ≥50 years
  • Post-menopausal if Female
  • BMI of 30-50 kg/m2 for ambulatory participants (less than or equal to 350 lbs.)
  • BMI of 25-50 kg/m2 for wheelchair users (less than or equal to 350 lbs.)
  • Ambulatory with or without a walking device or use of a manual wheelchair for mobility.

排除标准

  • Untreated hyper or hypothyroidism.
  • Cancer (except basal cell).
  • Gastrointestinal disorders affecting food intake.
  • <3 months of stable use of medications that affect metabolism, body weight, energy expenditure or appetite.
  • Current eating disorder (e.g., binge eating disorder, anorexia, or bulimia).
  • Any medical condition for which following a HP diet and/or 70 minutes of exercise daily would be inadvisable.
  • Uses a powered wheelchair for mobility.
  • Has a pacemaker or any other life-sustaining medical implant.

结局指标

主要结局

Class Attendance

时间窗: Baseline through week 52.

Class Attendance will be tracked to determine clinical trial feasibility.

2nd Stage Intervention Preference

时间窗: Week 8

Participant preferences for 2nd stage interventions will be measured at week 8 by answering a 5-point Likert question with '1' and '5' representing a strong preference for either intervention and '3' representing no intervention preference.

Recruitment and Retention Rates

时间窗: Baseline through week 52.

Rates of study recruitment and retention will be tracked to determine clinical trial feasibility.

1st Stage Intervention Preference

时间窗: Baseline

Participant preferences for 1st stage interventions will be measured at baseline by answering a 5-point Likert question with '1' and '5' representing a strong preference for either intervention and '3' representing no intervention preference.

1st Stage Treatment Credibility

时间窗: Baseline.

Perceived credibility of 1st stage interventions will be measured at baseline with the Credibility/Expectancy Questionnaire.

2nd Stage Treatment Credibility

时间窗: Week 8.

Perceived credibility of 2nd stage interventions will be measured in non-responders to 1st stage interventions at week 8 with the Credibility/Expectancy Questionnaire.

次要结局

  • Body Weight(Baseline, Weeks 8, 16, and 52)
  • Fat mass(Baseline, Weeks 8, 16, and 52)
  • Fat free mass(Baseline, Weeks 8, 16, and 52)

研究者

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

Drew Sayer

Primary Investigator

University of Alabama at Birmingham

研究点 (2)

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