Sit Less for Successful Aging
Sit Less for Successful Aging: A Sedentary Behavior Intervention for Older Adults in Independent Living Communities
調査の概要
詳細な説明
Aim 1: To measure the amount of sedentary time and ambulation (steps) in older adults residing in independent living communities.
Aim 2: To test the acceptability and effectiveness of a 12-week sedentary behavior intervention to decrease sitting and increase ambulation which will in turn improve physical function (primary outcome) as well as sleep, quality of life, energy/mood, pain and blood pressure (secondary outcomes) in independent living residents.
Background: Sedentary behavior, or sitting for prolonged periods during waking time, is identified as a health risk that is distinct from the failure to achieve sufficient physical activity. Older adults exhibit the greatest time in sedentary behavior which is concerning given its association with chronic disease and poorer physical function. Preliminary data suggest that individuals in long term care facilities may have even greater sedentary time due to personal factors and environment influences. Most often, exercise is targeted as a mechanism for ameliorating frailty in older adults; however, reduction in sedentary time may be a more appealing and realistic goal for improving health outcomes. Despite this, studies targeting sedentary time in older adults, particularly in those in independent living facilities, are lacking.
研究の種類
入学 (実際)
段階
- 適用できない
連絡先と場所
研究場所
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Pennsylvania
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Pittsburgh、Pennsylvania、アメリカ、15219
- University of Pittsburgh
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-
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 ≥ 60 years
- Reside in an independent living facility
- Ability to walk approximately 100 feet (length of a hallway) with or without an assistive device
Exclusion Criteria:
- Unable to provide informed consent
- Presence of a comorbid medical condition that would limit ability to stand and perform light activity (e.g. recent orthopedic injury/surgery involving the lower extremities, currently undergoing treatment for cancer,acute cardiovascular conditions)
- Presence of a skin condition that would prohibit the use of an activity device attached with medical tape to the thigh (e.g. open wound on the thigh, skin infection on the lower extremity)
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：処理
- 割り当て：なし
- 介入モデル：単一グループの割り当て
- マスキング：なし（オープンラベル）
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
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実験的：Sedentary Behavior Intervention
A behavioral intervention that targets prolonged sitting and encourages frequent activity breaks.
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This 12-week intervention targets a reduction in prolonged sitting and includes provision of a wrist-worn activity prompter and in-person group sessions with behavioral counseling.
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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 |
|---|---|---|
|
Change in Sedentary Behavior
時間枠：Baseline to 12 weeks
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Objectively measured minutes of sitting during waking hours measured using the ActivPAL physical activity monitor for a minimum of 5 days pre and post-intervention.
The ActivPAL is a thigh-mounted, compact device that classifies an individual's free-living activity into time spent in sedentary, standing, and walking behaviors.
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Baseline to 12 weeks
|
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Steps per Day
時間枠：Baseline to 12 weeks
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The number of steps per day measured using the ActivPAL activity monitor.
This monitor is worn for a minimum of 5 days before and after the intervention.
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Baseline to 12 weeks
|
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Short Physical Performance Battery
時間枠：Baseline to 12 weeks
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This performance-based measure of physical function is a battery of measures to assess standing balance, gait speed and lower extremity strength (time to complete five chair rises)
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Baseline to 12 weeks
|
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Patient Reported Outcomes Measurement Information System (PROMIS) Physical Function Short Form 10a
時間枠：Baseline to 12 weeks
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This self-report measure of physical function has 10 questions that assess the ability to perform various activities that require physical capability.
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Baseline to 12 weeks
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協力者と研究者
スポンサー
捜査官
- 主任研究者：Andrea L Hergenroeder, PT, PhD、Assistant Professor, Department of Physical Therapy
研究記録日
主要日程の研究
研究開始 (実際)
一次修了 (実際)
研究の完了 (実際)
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
その他の研究ID番号
- 17020397
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?
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米国FDA規制医薬品の研究
米国FDA規制機器製品の研究
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