青少年および若年成人の体重増加予防
青少年および若年成人の肥満の予防
The investigators believe they key to effective prevention of obesity is early identification of individuals at high risk of excess weight gain and proactive implementation of a comprehensive approach including lifestyle-based coaching and preventive medical management targeting the pathophysiology of dysregulated energy metabolism. In this study the investigators will take a fundamentally different approach to the science of obesity prevention by targeting the underlying biological processes driving unhealthy weight gain in adolescents/young adults (AYAs), a group that has been underrepresented in medication trials.
調査の概要
詳細な説明
Once obesity develops and becomes entrenched, achieving sustained weight loss is extremely difficult. Thus, preventing the accumulation of excess adiposity in high-risk individuals is the ideal course of action. AYAs are high-risk individuals, as this is a life stage characterized by susceptibility for accelerated weight gain. However, most obesity prevention interventions targeting AYAs have reported null findings or modest effects. It is possible that failure to address the underlying physiology of the energy regulatory system is at least partly responsible for the underwhelming results. Numerous physiological mechanisms drive weight gain by stimulating appetite and food palatability, as well as influence other weight related behaviors to achieve a predetermined body weight set point. Previous obesity prevention interventions in AYAs have almost entirely focused on modifying individual behaviors and/or external environmental conditions and have not addressed the biological pathways driving energy regulation. Effectively targeting the underlying physiological processes promoting body fat storage, such as with pharmacotherapy, may be an essential component of successful obesity prevention for some individuals.
When used in combination with lifestyle-based weight gain prevention counseling, low-dose preventative pharmacotherapy has the potential to halt or slow unhealthy weight gain in AYAs by targeting key mechanisms in the energy regulatory system. Qsymia is among the most cost-effective anti-obesity medications approved for adolescents and adults. Its mechanisms of action may be ideal for impeding weight gain and ultimately preventing the onset of obesity because they are multifactorial and involve reducing appetite, enhancing satiety, and potentially increasing energy expenditure. Moreover, flexible dosing with Qsymia provides the option to introduce preventative pharmacotherapy at low levels of exposure (minimizing risk) yet allows for dose escalation if weight gain were to ensue. It is also attractive in the context of prevention owing to its oral route of administration and relatively low cost compared to other medications.
In the proposed clinical trial, the investigators plan to diverge significantly from historical obesity prevention approaches by pairing lifestyle-based weight gain prevention coaching with low-dose preventative pharmacotherapy to target the underlying biological processes implicated in weight gain. The investigators will target AYAs (18 to <25 years old) at high risk of developing obesity: defined as those with a body mass index (BMI) between 25-29.9 kg/m^2 (overweight classification) and a family history of obesity (one biological parent with severe obesity and/or two biological parents with obesity). The investigators will randomize 140 of these individuals (1:1) to Qsymia or placebo with both groups additionally receiving lifestyle-based weight gain prevention coaching. Over a period of two years, the investigators will: 1) compare changes between groups in BMI trajectories as well as incidence of obesity and regression to normal weight; 2) determine if there are differences between groups in diet quality and eating behaviors; and 3) investigate changes in visceral adipose tissue and its relation to cardiometabolic risk.
研究の種類
入学 (推定)
段階
- フェーズ 3
連絡先と場所
研究連絡先
- 名前:Aaron Kelly, PhD
- 電話番号:(612) 626-3492
- メール:kelly105@umn.edu
研究連絡先のバックアップ
- 名前:Lisa Hostetler
- 電話番号:(612) 6253261
- メール:hoste005@umn.edu
研究場所
-
-
Minnesota
-
Minneapolis、Minnesota、アメリカ、55414
- 募集
- University of Minnesota Center for Pediatric Obesity Medicine
-
コンタクト:
- Samira Ahmed
- メール:ahmed787@umn.edu
-
主任研究者:
- Aaron Kelly, PhD
-
-
参加基準
適格基準
就学可能な年齢
健康ボランティアの受け入れ
受講資格のある性別
説明
Inclusion Criteria:
- Age 18 to M 25 at screening
- BMI >/= 25 to < 30 kg/m^2
- Family history of obesity defined as one biological parent with severe obesity (BMI >/= 35) and/or two biological parents with obesity (BMI >/=30). Parental obesity status will be confirmed by obtaining a release of information to review and electronic health record.
Exclusion Criteria:
- Tanner stage 1-4
- Diabetes (type 1 or 2)
- Current or recent (<6 months prior to screening) use of anti-obesity medication(s) or other weight-altering medication(s) (e.g. atypical anti-psychotics, attention deficit hyperactivity disorder (ADHD) stimulant)
- Previous bariatric surgery
- Current or recent (<6 months prior to screening) use of medication(s) to treat insulin resistance
- Recent initiation (<3 months prior to screening) of anti-hypertensive or lipid medication(s)
- History of glaucoma
- Current or recent (<14 days prior to screening) use of monoamine oxidase inhibitor
- Known hypersensitivity to sympathomimetic amines
- History of treatment with growth hormone
- Patient Health Questionnaire-9 (PHQ-9) score of >/= 15 at screening
- Eating disorder symptoms within 6 months and/or any past medical diagnosis of eating disorder
- Major psychiatric disorder
- Unstable clinically-diagnosed depression
- History of suicide attempt
- Suicidal ideation of type 4 or 5 on the Columbia-Suicide Severity Rating Scale (C-SSRS) at any time during the study
- Current pregnancy or breastfeeding
- Plans to become pregnant
- If sexually active, refusal to use 2 forms of birth control
- Tobacco use
- Alanine transaminase (ALT) or aspartate transaminase (AST) >/= 2.5 times the upper limit of normal
- Bicarbonate 18 mmol/L
- Creatinine > 1.2 mg/dL
- Creatinine clearance <50 mL/min (Schwartz formula)
- History of seizures
- Uncontrolled hypertension
- History of structural heart defect
- History of clinically significant arrhythmia
- Diagnosed monogenic obesity
- History of cholelithiasis
- History of nephrolithiasis
- Hyperthyroidism
- Untreated thyroid disorder
研究計画
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:防止
- 割り当て:ランダム化
- 介入モデル:並列代入
- マスキング:ダブル
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
|
実験的:Qsymia arm
Qsymia |
Qsymia
他の名前:
|
|
プラセボコンパレーター:Placebo arm
Placebo |
Placebo |
この研究は何を測定していますか?
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
BMI
時間枠:24 months
|
Change in body mass index |
24 months
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Diet quality and eating behaviors
時間枠:24 months
|
Daily caloric intake |
24 months
|
協力者と研究者
スポンサー
捜査官
- 主任研究者:Aaron Kelly, PhD、University of Minnesota
研究記録日
主要日程の研究
研究開始 (推定)
一次修了 (推定)
研究の完了 (推定)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
本研究に関する用語
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
IPD プランの説明
A long-term data sharing and preservation plan will be used to store and make publicly accessible the data beyond the life of the project. The deidentified data will be deposited into the Data Repository for University of Minnesota (DRUM). This University of Minnesota Libraries hosted institutional data repository is an open access platform for dissemination and archiving of university research data and is free to the University of Minnesota researchers. Curators review all incoming submissions and work with data authors to comply with data sharing requirements in ways that make data FAIR (Findable, Accessible, Interoperable, Reusable).
IPD 共有時間枠
10 years
IPD 共有アクセス基準
U of Minnesota Libraries
IPD 共有サポート情報タイプ
- STUDY_PROTOCOL
- SAP
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
米国FDA規制機器製品の研究
この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。