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Facebook to Promote Physical Activity in Black Women African American Women

2015年2月25日 更新者:Barbara E. Ainsworth、Arizona State University

Using Mass Media to Promote Physical Activity in African American Women

The purpose of this study is to evaluate the feasibility of a social media and text-message-delivered, Social Cognitive Theory-based, culturally relevant intervention designed to promote physical activity among African American women. An 8-week, 2-arm randomized trial will be implemented. Arm 1 will receive a culturally-relevant, technology-based physical activity intervention delivered via Facebook and text messages. Arm 2 (Comparison Group) will receive a standard print-based physical activity promotion materials consisting of high quality physical activity promotion brochures produced by the American Heart Association.

調査の概要

詳細な説明

The purpose of this study is to apply and investigate the feasibility of a social media and text-message-delivered, Social Cognitive Theory-based, culturally relevant intervention designed to promote physical activity among African American women. In an 8-week, 2-arm randomized trial, 30 African American women will be assigned to receive either: a) culturally-relevant, technology-based physical activity intervention delivered via Facebook and text messages, or b) a standard print-based physical activity promotion intervention consisting of high quality physical activity promotion brochures produced by the American Heart Association delivered via USPS mail.

Aim 1: Test the feasibility of a culturally relevant, social media and text-message delivered physical promotion pilot intervention among adult African American women. The investigators hypothesize that the culturally relevant Facebook and text message delivered intervention will be feasible as measured by the acceptability, implementation, and practicality of the intervention program.

Aim 2: Examine the impact of the culturally-relevant, Facebook and text message delivered intervention to increase physical activity and enhance associated Social Cognitive Theory constructs explicitly targeted by the intervention activities. Physical activity will be objectively measured by accelerometers and Social Cognitive Theory constructs of self-efficacy, social support, self-regulation, and outcome expectations will be assessed by validated self-report questionnaires. The investigators hypothesize that participants receiving the culturally-adapted, Social Cognitive Theory-based Facebook and text-message intervention will demonstrate higher physical activity levels and greater enhancements in Social Cognitive Theory constructs when compared to the standard print-based intervention group at the post-intervention assessment.

Aim 3: Examine the preliminary effect of a culturally relevant, social media-delivered physical activity promotion intervention on anthropometric, blood pressure, and blood lipid outcomes. The investigators hypothesize that increased physical activity at the post-intervention follow-up will be associated with improvements in these variables.

研究の種類

介入

入学 (実際)

30

段階

  • 適用できない

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

24年~49年 (大人)

健康ボランティアの受け入れ

はい

受講資格のある性別

女性

説明

Inclusion Criteria:

  • self-identified as African American
  • female
  • insufficiently active (<150 min/week of moderate-intensity physical activity assessed by the short version of the International Physical Activity Questionnaire)
  • aged 24-49 years
  • having an active Facebook account
  • ability to read/write in English

Exclusion Criteria:

  • concurrent participation in another physical activity promotion program (research or commercial)
  • being pregnant or planning on becoming pregnant in the next 6 months, and
  • self-reported condition that inhibits engagement in physical activity
  • contraindication for physical activity according to the Physical Activity Readiness Questionnaire (PAR-Q) unless written permission from the participant's physician to engage in the study is provided

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

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: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
実験的:Facebook and Text Message
Participants randomized to the technology-based physical activity intervention will receive a culturally-relevant physical activity promotion intervention delivered via text messages and the social media website Facebook. The purpose of the intervention materials is to encourage participants to achieve a minimum of 150 minutes/week of moderate-intensity aerobic physical activity each week.
Culturally-relevant physical activity promotion program
アクティブコンパレータ:Standard Print-based Intervention
Participants randomized to the standard print-based physical activity intervention group will be mailed 4 self-help booklets promoting physical activity produced by the American Heart Association. Booklets will be mailed one at a time in 2 week intervals over the 1st 6-weeks of the intervention. These high quality booklets provide general information on the benefits of physical activity, tips and strategies to increase daily physical activity, and encourage recipients to perform a minimum of 10,000 steps per day.
Non-culturally relevant physical activity promotion program

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
Feasibility of Using Facebook and Text Messaging to Deliver a Physical Activity Program to African American Women
時間枠:Post Intervention (up to 8 weeks)
Measured using a composite score by assessing acceptability (participants perceived satisfaction and usefulness of the program; perceived cultural relevance of the program), demand (interest in study participation; participant retention), and implementation (participant activity on the Facebook group page, successful delivery of text messages, successful delivery of study materials on the study Facebook wall) of the culturally relevant physical activity program.
Post Intervention (up to 8 weeks)

二次結果の測定

結果測定
メジャーの説明
時間枠
Change in physical activity from baseline to 8 weeks
時間枠:Two assessments, 8 weeks apart
Assessed by ActiGraph GT3X+ accelerometers
Two assessments, 8 weeks apart
Change in exercise self-efficacy from baseline to 8 weeks
時間枠:Two assessments, 8 weeks apart
Assessed by the Exercise Confidence Survey (Sallis, 1988)
Two assessments, 8 weeks apart
Change in social support for exercise from baseline to 8 weeks
時間枠:Two assessments, 8 weeks apart
Assessed by the Social Support for Exercise Survey (Sallis,1987)
Two assessments, 8 weeks apart
Change in self-regulation for physical activity from baseline to 8 weeks
時間枠:Two assessments, 8 weeks apart
Assessed by the Self-Regulation Scale from the Health Beliefs Survey (Anderson, 2010)
Two assessments, 8 weeks apart
Change in outcome expectations for exercise from baseline to 8 weeks
時間枠:Two assessments, 8 weeks apart
Assessed by the Outcome Expectation Scale for Exercise (Resnick, 2000)
Two assessments, 8 weeks apart
Change in body mass index (BMI) from baseline to 8 weeks
時間枠:Two assessments, 8 weeks apart
Two assessments, 8 weeks apart
Change in total serum cholesterol from baseline to 8 weeks
時間枠:Two assessments, 8 weeks apart
Two assessments, 8 weeks apart
Change in serum high-density lipoprotein (HDL) cholesterol from baseline to 8 weeks
時間枠:Two assessments, 8 weeks apart
Two assessments, 8 weeks apart
Change in serum low-density lipoprotein (LDL) cholesterol from baseline to 8 weeks
時間枠:Two assessments, 8 weeks apart
Two assessments, 8 weeks apart
Change in serum triglycerides from baseline to 8 weeks
時間枠:Two assessments, 8 weeks apart
Two assessments, 8 weeks apart

協力者と研究者

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出版物と役立つリンク

研究に関する情報を入力する責任者は、自発的にこれらの出版物を提供します。これらは、研究に関連するあらゆるものに関するものである可能性があります。

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始

2014年3月1日

一次修了 (実際)

2014年6月1日

研究の完了 (実際)

2014年6月1日

試験登録日

最初に提出

2015年2月6日

QC基準を満たした最初の提出物

2015年2月25日

最初の投稿 (見積もり)

2015年2月26日

学習記録の更新

投稿された最後の更新 (見積もり)

2015年2月26日

QC基準を満たした最後の更新が送信されました

2015年2月25日

最終確認日

2015年2月1日

詳しくは

本研究に関する用語

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。

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