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A commercialized dietary supplement alleviates joint pain in community adults: a double-blind, placebo-controlled community trial.


ABSTRACT: The purpose of this study was to assess the effect of 8-weeks ingestion of a commercialized joint pain dietary supplement (Instaflex™ Joint Support, Direct Digital, Charlotte, NC) compared to placebo on joint pain, stiffness, and function in adults with self-reported joint pain. Instaflex™ is a joint pain supplement containing glucosamine sulfate, methylsufonlylmethane (MSM), white willow bark extract (15% salicin), ginger root concentrate, boswella serrata extract (65% boswellic acid), turmeric root extract, cayenne, and hyaluronic acid.Subjects included 100 men and women, ages 50-75 years, with a history (>3 months) of joint pain, and were randomized to Instaflex™ or placebo (3 colored gel capsules per day for 8 weeks, double-blind administration). Subjects agreed to avoid the use of non-steroidal anti-inflammatory drugs (NSAID) and all other medications and supplements targeted for joint pain. Primary outcome measures were obtained pre- and post-study and included joint pain severity, stiffness, and function (Western Ontario and McMaster Universities [WOMAC]), and secondary outcome measures included health-related quality of life (Short Form 36 or SF-36), systemic inflammation (serum C-reactive protein and 9 plasma cytokines), and physical function (6-minute walk test). Joint pain symptom severity was assessed bi-weekly using a 12-point Likert visual scale (12-VS).Joint pain severity was significantly reduced in Instaflex™ compared to placebo (8-week WOMAC, ?37% versus ?16%, respectively, interaction effect P?=?0.025), with group differences using the 12-VS emerging by week 4 of the study (interaction effect, P?=?0.0125). Improvements in ability to perform daily activities and stiffness scores in Instaflex™ compared to placebo were most evident for the 74% of subjects reporting knee pain (8-week WOMAC function score, ?39% versus ?14%, respectively, interaction effect P?=?0.027; stiffness score, ?30% versus ?12%, respectively, interaction effect P?=?0.081). Patterns of change in SF-36, systemic inflammation biomarkers, and the 6-minute walk test did not differ significantly between groups during the 8-week studyResults from this randomized, double blind, placebo-controlled community trial support the use of the Instaflex™ dietary supplement in alleviating joint pain severity in middle-aged and older adults, with mitigation of difficulty performing daily activities most apparent in subjects with knee pain.

SUBMITTER: Nieman DC 

PROVIDER: S-EPMC4176106 | biostudies-literature | 2013 Nov

REPOSITORIES: biostudies-literature

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A commercialized dietary supplement alleviates joint pain in community adults: a double-blind, placebo-controlled community trial.

Nieman David C DC   Shanely R Andrew RA   Luo Beibei B   Dew Dustin D   Meaney Mary Pat MP   Sha Wei W  

Nutrition journal 20131125 1


<h4>Background</h4>The purpose of this study was to assess the effect of 8-weeks ingestion of a commercialized joint pain dietary supplement (Instaflex™ Joint Support, Direct Digital, Charlotte, NC) compared to placebo on joint pain, stiffness, and function in adults with self-reported joint pain. Instaflex™ is a joint pain supplement containing glucosamine sulfate, methylsufonlylmethane (MSM), white willow bark extract (15% salicin), ginger root concentrate, boswella serrata extract (65% boswel  ...[more]

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