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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。 | ||
フィルター基準に一致する試験が1件見つかりました
タイル表示
Community Translation of the Expecting Study
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 は 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
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
副次評価項目
| 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 |
| 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.
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