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Short- and Long-Term Changes in Health-Related Quality of Life with Weight Loss: Results from a Randomized Controlled Trial.


ABSTRACT: OBJECTIVE:The objective of this study was to determine the effects of weight loss and weight loss maintenance (WLM) on weight-specific health-related quality of life in a 66-week trial. METHODS:Adults with obesity (N?=?137, 86.1% female, 68.6% black, mean age?=?46.1 years) who had lost???5% of initial weight in a 14-week intensive lifestyle intervention/low-calorie diet (LCD) program were randomly assigned to lorcaserin or placebo for an additional 52-week WLM program. The Impact of Weight on Quality of Life-Lite (IWQOL-Lite) scale (including five subscales), Patient Health Questionnaire-9 (depression), and Perceived Stress Scale were administered at the start of the 14-week LCD program, randomization, and week 52 of the randomized controlled trial (i.e., 66 weeks total). RESULTS:Significant improvements in all outcomes, except weight-related public distress, were found following the 14-week LCD program (P values

SUBMITTER: Pearl RL 

PROVIDER: S-EPMC5970047 | biostudies-literature | 2018 Jun

REPOSITORIES: biostudies-literature

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Short- and Long-Term Changes in Health-Related Quality of Life with Weight Loss: Results from a Randomized Controlled Trial.

Pearl Rebecca L RL   Wadden Thomas A TA   Tronieri Jena Shaw JS   Berkowitz Robert I RI   Chao Ariana M AM   Alamuddin Naji N   Leonard Sharon M SM   Carvajal Raymond R   Bakizada Zayna M ZM   Pinkasavage Emilie E   Gruber Kathryn A KA   Walsh Olivia A OA   Alfaris Nasreen N  

Obesity (Silver Spring, Md.) 20180420 6


<h4>Objective</h4>The objective of this study was to determine the effects of weight loss and weight loss maintenance (WLM) on weight-specific health-related quality of life in a 66-week trial.<h4>Methods</h4>Adults with obesity (N = 137, 86.1% female, 68.6% black, mean age = 46.1 years) who had lost ≥ 5% of initial weight in a 14-week intensive lifestyle intervention/low-calorie diet (LCD) program were randomly assigned to lorcaserin or placebo for an additional 52-week WLM program. The Impact  ...[more]

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