A Pharmacy-Based Observational Study of Digest-8 Dietary Supplement in a Consumer Healthcare Context.

Global advances in integrative medicine and health Pub Date : 2024-07-25 eCollection Date: 2024-01-01 DOI:10.1177/27536130241268240
Marc Brodsky, Josette Hartnett, Kaly Houston, Suzanne J Rose
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引用次数: 0

Abstract

Background: Functional gastrointestinal disorders (FGIDs), a frequent cause of gastrointestinal (GI) symptomology, impact 40%-69% of the United States population. People who suffer from FGIDs often self-manage their symptoms using consumer healthcare products such as dietary supplements.

Objective: To investigate use of Digest-8 dietary supplement by people who purchased the product from pharmacies for their FGID symptoms.

Methods: This pharmacy-based observational study included a convenience sample recruited by flyers at 2 pharmacies upon purchase of Digest-8 dietary supplement to assess symptoms, satisfaction, tolerability, and side-effects through 7 weekly voluntary surveys completed by consenting participants.

Results: Twenty-two participants completed an initial survey and a collective total of 59 follow-up surveys. Analysis of follow-up surveys compared to baseline provided pilot data on symptom improvement, satisfaction, tolerability, and low side effect profile.

Conclusion: Preliminary findings of the study warrant a follow-up prospective randomized clinical trial to address the study limitations.

以消费者保健为背景的 Digest-8 膳食补充剂药房观察研究。
背景:功能性胃肠紊乱(FGIDs)是导致胃肠道症状的常见原因,影响着 40%-69% 的美国人口。FGIDs患者通常会使用膳食补充剂等消费者保健产品来自我控制症状:调查从药店购买 Digest-8 膳食补充剂来治疗 FGID 症状的人的使用情况:这项以药房为基础的观察性研究包括在2家药房通过发传单招募购买Digest-8膳食补充剂的方便样本,通过每周7次由同意参与者自愿完成的调查来评估症状、满意度、耐受性和副作用:结果:22 名参与者完成了首次调查,总共完成了 59 次后续调查。对后续调查与基线调查的比较分析提供了有关症状改善、满意度、耐受性和低副作用的试验数据:该研究的初步结果证明,有必要进行后续的前瞻性随机临床试验,以解决研究的局限性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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