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治験 NCT04298125(対象:妊娠関連)は募集中です。詳細は治験レーダーのタイル表示と AI 発見ツールで確認するか、ここで質問してください。
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Community Translation of the Expecting Study

募集中
治験(臨床試験)の詳細は主に英語で提供されています。しかし、治験レーダーAIが支援できます!「治験を説明」をクリックして、選択した言語で試験情報を表示し、議論してください。
治験番号 NCT04298125介入研究 臨床試験 で、妊娠関連 に関するものです。現在は 募集中 で、2021年7月16日 から開始しています。60 名の参加者 の募集が計画されています。この治験は Arkansas Children's Hospital Research Institute によって主催され、2026年6月1日 に完了予定です。ClinicalTrials.gov からの最新更新日は 2025年10月2日 です。
概要
The Expecting intervention as delivered in prior studies in a clinical setting is described in a previous approved IRB submission (Protocol 202954). The current project will seek to engage community stakeholders to translate Expecting to a community-delivered intervention and to test its acceptability, feasibility, and fidelity in a proof of principle study with 60 expecting mothers.
詳細説明
The aim of this study is to adapt and determine acceptability, feasibility and fidelity of the research- clinic-based Expecting intervention with pregnant women with obesity in community settings. Specifically, the investigators will show effective application of the Replicating Effective Programs (REP) framework (e.g., fidelity, feasibility, acceptability) to translate the research clinic-based intervention to community settings. REP provides a four-phase process for implementing evidence-based interventions and has demonstrated effective application to translate clinical interventions to community settings. Built into the REP framework is the collection of feedback from community stakeholders, iterative piloting of the intervention in the community, and a process for standardizing the intervention across community settings. Following adaptation, the updated intervention will be piloted. The pilot study will include 60 expecting women. The investigators will randomize half to receive the community-adapted Expecting intervention (Intervention, N=30) and half to receive standard of care (Control, N=30).
公式タイトル

Antenatal Factors Impacting Obesity and Metabolism in Children: Sub-objective 2D

疾患/病気
妊娠関連
刊行物
この臨床試験について発表された科学記事と研究論文:
その他の研究識別子
  • 260132
NCT番号
開始日
2021-07-16
最終更新日
2025-10-02
終了予定日
2026-06
目標参加者数
60
試験の種類
介入研究
治験の相・段階
該当なし
状況
募集中
主目的
予防
割付方法
無作為化
介入モデル
並行割当
盲検化
単盲検
群(アーム)/介入
参加グループ/群介入/治療法
実験的Exercise in Pregnancy in Community
The Expecting intervention at the ACNC includes three 30-45 minute, in-person exercise sessions per week. The sessions are gradually increased in length over the first weeks of participation, and are comprised of 15-30 minutes of moderate aerobic activity (recumbent bike, walking on a treadmill or on an elliptical machine) as well as 5-10 minutes of resistance training using hydraulic exercise equipment. The sessions conclude with stretching exercises. Throughout the session, a personal trainer assesses the rating of perceived exertion using the 6 to 20 point Borg scale of exhaustion.41 Between sessions, participants are asked to monitor their daily step count with a target of 10,000 steps per day using a pedometer provided to the participant. This number is reported to or downloaded by the personal trainer at each in-person session. These elements will be adapted to provide a similar exercise experience that is accessible to women in their local community.
Exercise in Pregnancy
Women in this group will participate in psychical activity 3 times per week in their community setting.
非介入Standard Care
Participants will receive guidance on exercise from their physician as usual.
該当なし
主要評価項目
評価指標指標の説明時間枠
Feasibility of Intervention Measure:38 weeks
Attitudinal Implementation Outcome on a 1 to 5 scale
38 weeks
Acceptability of Intervention Measure: 38 weeks
Attitudinal Implementation Outcome on a 1 to 5 scale
38 weeks
副次評価項目
評価指標指標の説明時間枠
Number of intervention sessions completed
Measured with attendance records
15 weeks through 38 weeks
Number of minutes of physical activity
Measured with Actical
Change from Baseline to Delivery and 6 Months Post Delivery
Body Mass Index
Collected from Medical Record, weight and height will be combined to report BMI in kg/m\^2
Change from Baseline to Delivery and 6 Months Post Delivery
Blood Pressure
Collected from Medical Record
Change from Baseline to Delivery and 6 Months Post Delivery
Total Cholesterol from Lipid Panel
Collected from Medical Record
Change from Baseline to Delivery and 6 Months Post Delivery
適格基準

対象年齢
成人, 高齢者
試験の最低年齢
18 Years
対象性別
女性
  • (a) Body Mass Index > 30,
  • (b) singleton pregnancy,
  • (c) between 11-15 weeks of pregnancy (at enrollment),
  • (d) Do not currently meet recommended guidelines of 150 min of activity per week
  • (e) cleared by physician

  • (a) contraindications for exercise (preeclampsia-eclampsia, premature rupture of the membranes, antepartum hemorrhage, placenta previa, multiple gestation and other defined conditions)
  • (b) illicit drug use.
Arkansas Children's Hospital Research Institute logoArkansas Children's Hospital Research Institute
試験中央連絡先
連絡先: Taren Swindle, PhD, 501-526-7058, [email protected]
1 1カ国の場所

Arkansas

Arkansas Children's Nutrition Center, Little Rock, Arkansas, 72205, United States
Taren M Swindle, PhD, 連絡先
募集中