Social Worker in an Eye-Care Service
The Impact of a Social Worker in a Glaucoma Eye-Care Service: A Prospective Study
調査の概要
状態
条件
詳細な説明
An appointment will be scheduled for participant to meet with a social worker. The appointment may happen on day of participant's scheduled clinic appointment or on another mutually decided upon date and time. Should participant choose to participate, this first visit will be Visit 1 for the study.
Visit 1: Baseline
Informed consent will be obtained demonstrating an interest in participating.
A visit with the social worker will take place during Visit 1. This session will be held in a private office and allows participant time for discussion regarding any challenges, struggles and/or barriers they may be experiencing.
The following baseline questionnaires/surveys will be administered:
Modified Patient Activation Measure - measures participant confidence in taking care of their own health.
Distress Thermometer - measures participant distress level during the past week.
Patient Health Questionnaire -measures depression symptoms and severity if any.
Clinical information will be taken from participant's medical record. There may be follow-up questions related to data if information is unclear or incomplete.
Upon completion of Visit 1, participant will receive a satisfaction survey to evaluate how participant satisfaction with social worker interaction.
Social Worker Interventions: After Visit 1 and before Visit 2
The social worker will develop an intervention for participant during Visit 1 appointment. As many calls or in person meetings participant requires will take place. There will be no limit and it will be determined by participant's needs.
Visit 2: Follow-up After 6 Months
Upon completion of participant's six month follow-up in the study, the following questionnaires/surveys will be administered:
Modified Patient Activation Measure - measures how confident participant is at taking care of their own health.
Distress Thermometer - measures how much distress participant has been experiencing in the past week.
Patient Health Questionnaire - measures if participant has symptoms of depression and the severity of those symptoms.
Satisfaction Survey - measures how satisfied participant is with the social worker interaction.
研究の種類
入学 (実際)
連絡先と場所
研究場所
-
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Pennsylvania
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Philadelphia、Pennsylvania、アメリカ、19107
- Wills Eye Hospital
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-
参加基準
適格基準
就学可能な年齢
- 子
- 大人
- 高齢者
健康ボランティアの受け入れ
受講資格のある性別
サンプリング方法
調査対象母集団
説明
Inclusion Criteria:
- Patients seen at Wills Eye Hospital in the Glaucoma Service
- Glaucoma of any type, characterized by glaucomatous optic neuropathy and corresponding visual field (VF) defect
- Referred to staff social worker for intervention
- Ability to read, write, speak and understand English
Exclusion Criteria:
- None
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
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 response to Patient Health Questionnaire 9
時間枠：6 months
|
Measures participant levels of depression based on questions related to depressive symptoms.
The investigator will assess change in the number of participants with major, moderate, and minimal depressive symptoms.
|
6 months
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Change in response to Distress thermometer
時間枠：6 months
|
Measures participant level of distress on a scale of 1 to 10 and asks additional questions regarding contributors to distress.
|
6 months
|
|
Change in response to Modified Patient Activation Measure 13
時間枠：6 months
|
Measures participant self-capacity for and confidence regarding glaucoma management.
|
6 months
|
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Descriptive results of the Social Worker Baseline Assessment
時間枠：6 months
|
Social worker will assess each participant's internal and external barriers to care, limitations, and strengths that may help them to manage their glaucoma.
|
6 months
|
協力者と研究者
スポンサー
捜査官
- 主任研究者：Scott J Fudemberg, MD、Wills Eye Hospital
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
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
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?
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。