Breathe With Ease: A Unique Approach to Managing Stress (BEAMS)
Improving Asthma Outcomes Through Stress Management
Uncontrolled asthma in at-risk youth responds well to guideline-based therapy when patients remain adherent to their management plans. Adherence to inhaled corticosteroids (ICS), when indicated for persistent or uncontrolled asthma, is a critical component of most asthma management plans, and other self-management practices such as trigger avoidance are similarly related to improved asthma outcomes. Adherence to self-management practices is mediated by multiple factors, including psychosocial stress of parents and their children.
A targeted, culturally appropriate intervention to manage psychosocial stress among the parents of young, African American, and socioeconomically disadvantaged urban children with asthma who are receiving guideline-based care may improve asthma self-management, and therefore asthma outcomes.
Our overall aim is to implement and evaluate a highly collaborative, multi-dimensional, culturally appropriate and community-based asthma intervention to augment existing guideline-based best practice. The intervention will target the parents of at-risk, urban, African American youth, and will employ individualized psychosocial stress management and peer support.
調査の概要
詳細な説明
Uncontrolled asthma in at-risk youth responds well to guideline-based therapy when patients remain adherent to their management plans. Adherence to inhaled corticosteroids (ICS), when indicated for persistent or uncontrolled asthma, is a critical component of most asthma management plans, and other self-management practices such as trigger avoidance are similarly related to improved asthma outcomes. Adherence to self-management practices is mediated by multiple factors, including psychosocial stress of parents and their children.
A targeted, culturally appropriate intervention to manage psychosocial stress among the parents of young, African American, and socioeconomically disadvantaged urban children with asthma who are receiving guideline-based care may improve asthma self-management, and therefore asthma outcomes.
Our overall aim is to implement and evaluate a highly collaborative, multi-dimensional, culturally appropriate and community-based asthma intervention to augment existing guideline-based best practice. The intervention will target the parents of at-risk, urban, African American youth, and will employ individualized psychosocial stress management and peer support.
We will conduct a single blind, prospective randomized controlled trial comparing the IMPACT DC Asthma Clinic's existing intervention of guideline-based clinical care, education, and short-term care coordination (usual care) to usual care plus parental stress management in a cohort of up to 200 parent-child dyads of AA youth aged 4-12 years.
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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District of Columbia
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Washington、District of Columbia、アメリカ、20010
- Children's National Medical Center
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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
We plan to enroll parent-child dyads that meet the following criteria:
Inclusion criteria (Parent):
- self-identify as African-American
- both the legal guardian and primary asthma caregiver of an eligible child.
Exclusion criteria (Parent):
- unable or unwilling to sign informed consent document
- exclusionary psychiatric condition, including but not limited to psychosis, based on the screening form at recruitment
- enrolled in another asthma research study.
Inclusion criteria (Child):
- parent-identified as African-American
- age 4-12 years inclusive at recruitment
- physician diagnosis of persistent asthma
- publicly financed insurance
Exclusion criteria (Child):
- chronic medical condition (other than asthma) including but not limited to diabetes, sickle cell disease, heart disease, lung disease or neurological disorder.
In addition, the PI may choose to not include a participant if he does not believe it is in the family's best interest to participate.
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：ランダム化
- 介入モデル：並列代入
- マスキング：独身
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
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アクティブコンパレータ：Usual Care
IMPACT DC Asthma Clinic intervention of guideline-based clinical care, education, and short-term care coordination
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IMPACT DC Asthma Clinic intervention of guideline-based clinical care, education, and short-term care coordination
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実験的：Intervention
Parental stress management in addition to IMPACT DC intervention of guideline-based clinical care, education, and short-term care coordination.
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The intervention for this study is a multi-dimensional stress management program designed to be responsive to parent and other stakeholder preferences.
The intervention will have two separate yet coordinated components: one-on-one stress management sessions and peer group sessions led by "community wellness coaches."
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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 |
|---|---|---|
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Symptom-free Days in the Last 14 Days
時間枠：Repeated Measures at 6 months (3 month data collected to allow for repeated measures)
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Symptom-free days are defined as a 24-hour period with no coughing, wheezing, chest tightness, or shortness of breath and no need for rescue medications
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Repeated Measures at 6 months (3 month data collected to allow for repeated measures)
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二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Asthma Morbidity - Nighttime Asthma Symptoms
時間枠：Repeated Measures at 6 and 12 months (3m data collected for repeated measures)
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Nights of asthma symptoms in prior 14d
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Repeated Measures at 6 and 12 months (3m data collected for repeated measures)
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Asthma Severity and Control
時間枠：Repeated Measures at 3, 6, and 12 months
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Repeated Measures at 3, 6, and 12 months
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Asthma Medication Adherence
時間枠：Repeated Measures at 6 and 12 months (3m data collected for repeated measures)
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Reported use of inhaled corticosteroids and LTRA in past two days
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Repeated Measures at 6 and 12 months (3m data collected for repeated measures)
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Health Care Utilization - Emergency Department Visits for Asthma
時間枠：12 months after enrollment
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Health care utilization - emergency department visits for asthma over six month and twelve month follow up periods.
Reported as those documented in the electronic medical record of Children's National Health System plus parent report of visits elsewhere
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12 months after enrollment
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Asthma Exacerbations - Courses of Systemic Steroids
時間枠：Assessed at 6m and 12m following enrollment
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Courses of systemic steroids over 12m follow up period
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Assessed at 6m and 12m following enrollment
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Parental Stress
時間枠：Repeated Measures at 6 and 12 months (3m data collected for repeated measures)
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Score on Perceived Stress Scale (PSS).
The Perceived Stress Scale consists of 10 questions and is a measure of the degree to which situations in one's life are appraised as stressful.
Scores range from 0 - 40, with higher scores indicating a higher level of perceived stress.
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Repeated Measures at 6 and 12 months (3m data collected for repeated measures)
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Parental Depression
時間枠：Repeated Measures at 6 and 12 months (3m data collected for repeated measures)
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Score on Center for Epidemiologic Studies Depression Scale (CES-D - 10).
The CESD-10 scale screens for depressive symptoms.
Scores range from 0-30, with higher scores indicating a higher degree of depressive symptoms.
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Repeated Measures at 6 and 12 months (3m data collected for repeated measures)
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Child Anxiety
時間枠：Repeated Measures at 6 and 12 months (3m data collected for repeated measures)
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PROMIS Parent Proxy Anxiety.
For PROMIS instruments, T-scores rescale the raw score into a standardized score with a mean of 50 and a standard deviation of 10.
A higher T-score represents higher anxiety and/or depression.
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Repeated Measures at 6 and 12 months (3m data collected for repeated measures)
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Child Depression
時間枠：Repeated Measures at 6 and 12 months (3m data collected for repeated measures)
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PROMIS Parent Proxy Depressive Symptoms is a parent-report assessment of child depression.
For PROMIS instruments, T-scores rescale the raw score into a standardized score with a mean of 50 and a standard deviation of 10.
A higher T-score represents higher anxiety and/or depression.
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Repeated Measures at 6 and 12 months (3m data collected for repeated measures)
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Caregiver Quality of Life
時間枠：Repeated Measures at 6 and 12 months (3m data collected for repeated measures)
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Caregiver quality of life score, assessed by modified Pediatric Asthma Caregiver Quality of Life Questionnaire (PACQLQ).
The measure had five response options, with scores ranging from 13-65 and higher scores meaning better quality of life.
No subscales were analyzed.
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Repeated Measures at 6 and 12 months (3m data collected for repeated measures)
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Number of Participants With AEs and SAEs
時間枠：12m follow up period
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Safety data: Number of Participants with AEs and SAEs
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12m follow up period
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Economic Outcomes
時間枠：12m follow-up period
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Analysis of costs of care in both groups
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12m follow-up period
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Caregiver Smoking Behavior
時間枠：Repeated Measures at 6 and 12 months
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parent report of cigarettes smoked per day
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Repeated Measures at 6 and 12 months
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Coping Strategies
時間枠：Repeated measures at 12m FU (6m data used for repeated measures)
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Brief COPE
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Repeated measures at 12m FU (6m data used for repeated measures)
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Mindfulness
時間枠：Repeated Measures at 6 and 12 months
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Interpersonal Mindfulness in Parenting
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Repeated Measures at 6 and 12 months
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Parental Resilience
時間枠：Repeated Measures at 6 and 12 months
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Parental resilience assessed by score on Revised Life Orientation Test (LOT-R) measure.
The LOT-R assesses optimism/resilience, and is comprised of 10 questions.
Scores range from 0-40, with a higher score indicating a higher level of optimism.
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Repeated Measures at 6 and 12 months
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Exacerbations - Hospital Admissions
時間枠：Assessed at 6m and 12m after enrollment
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Number of participants with hospital admissions due to exacerbations
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Assessed at 6m and 12m after enrollment
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Symptom-free Days in the Last 14 Days
時間枠：Repeated Measures at 12 months (with data also assessed at 3m and 6m)
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Symptom-free days are defined as a 24-hour period with no coughing, wheezing, chest tightness, or shortness of breath and no need for rescue medications
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Repeated Measures at 12 months (with data also assessed at 3m and 6m)
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Asthma Morbidity - Daytime Asthma Symptoms, Days of Activity Limitations, and Days of Quick Relief Medicine Use
時間枠：Repeated measures at 6 and 12 months (3m data collected for repeated measures)
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Days of asthma symptoms, activity limitation, and quick relief medicine use in prior 14d
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Repeated measures at 6 and 12 months (3m data collected for repeated measures)
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その他の成果指標
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Sociodemographics
時間枠：Baseline
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Age, gender, race, ethnicity, insurance type, parental education, household income, family medical history
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Baseline
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Number of Participants With Positive Smoke Exposure
時間枠：Repeated Measures at 6 and 12 months (3m data collected for repeated measures)
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Participants with environmental smoke exposure.
Responses were regrouped as negative (none) or positive (daily, often, or rarely) based on two questions: "How often did anyone smoke inside the home where child usually lives?" or "How often did anyone smoke in the room where child usually sleeps?"
A positive response on either or both questions was considered positive exposure.
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Repeated Measures at 6 and 12 months (3m data collected for repeated measures)
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Parental Health Literacy
時間枠：Baseline
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Single Item Literacy Screener (SILS)
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Baseline
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Use of Existing Ancillary Services
時間枠：Assessed at 6m and 12m following enrollment
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Assessed at 6m and 12m following enrollment
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Parental Resilience
時間枠：Baseline
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Parental resilience assessed by score on Revised Life Orientation Test (LOT-R) measure.
The LOT-R assesses optimism/resilience, and is comprised of 10 questions.
Scores range from 0-40, with a higher score indicating a higher level of optimism.
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Baseline
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Intervention Component Uptake
時間枠：6 month intervention period
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Completion of intervention sessions
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6 month intervention period
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Intervention Satisfaction
時間枠：6 month intervention period
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Brief survey of satisfaction with intervention components.
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6 month intervention period
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Intervention Fidelity
時間枠：6 month intervention period
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Checklist of staff's fidelity to individual components of intervention protocol
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6 month intervention period
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協力者と研究者
捜査官
- 主任研究者：Stephen Teach, MD, MPH、Children's National Health System
出版物と役立つリンク
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 (見積もり)
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
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