Pathways to Employment for the Long-term Unemployed
Pathways to the Labor Market for Long-term Unemployed: a Comparison of Labor Market Interventions Effects Mechanisms and Implementation
調査の概要
詳細な説明
Long-term unemployment has a profound impact on the health and wellbeing of individuals, families, and communities. In addition, the effects of long-term unemployment have been found to impact subgroups differently. Today there is scant knowledge on the mechanisms that are influential in moving individuals from long-term unemployment closer to the labor market. This study is designed to answer six research questions using a variety of methods (mixed-methods) and outcome measures (self-report, official register). In addition, this study leverages official register data to construct an untreated control group. This study will assess the extent to which an emerging theory of becoming job ready holds under experimental scrutiny.
This project will engage ALMP program administrators and service providers in semi-structured interviews. A total of 6 competing ALMPs will be included in the study. The transcribed interview material will be used as a basis for program theory reconstruction. All specified program theories will be presented back to program stakeholders for validation. ALMP program effectiveness will be assessed quasi-experimentally with pre- (T1) and posttest (T2) collection of self-reported data. Additionally, official register data from the Longitudinal integrated database for health insurance and labor market studies (LISA) will be collected for all participants. In addition, a matched sample will be collected from LISA to be used as a non-treated control group on final policy outcomes (e.g., employment, salary/wage). This study also assesses program implementation and economic outcomes of competing the competing ALMPs.
研究の種類
入学 (予想される)
連絡先と場所
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
サンプリング方法
調査対象母集団
説明
Inclusion Criteria:
- Unemployed for a period of at least 6 months, and
- 25 years old or younger, or
- born outside of Sweden, or
- 55 years old or older without higher education, or
- has a disability (physical, intellectual, neuropsychiatric, or mental) and
- receives social insurance benefits, or
- receives social welfare benefits
Exclusion Criteria:
- referred for services primarily by the Department of Justice
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
コホートと介入
グループ/コホート |
介入・治療 |
|---|---|
|
Municipal
Individual participants receiving active labor market intervention from municipal providers
|
Behavior change intervention
|
|
Non-profit
Individual participants receiving active labor market intervention from non-profit providers
|
Behavior change intervention
|
|
Register
Matched sample from register data, no intervention provided
|
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 employment and earnings
時間枠：baseline, 6 months post baseline
|
Employment and earnings data collected from official register data
|
baseline, 6 months post baseline
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Change in general health
時間枠：baseline, 6 months post baseline
|
Self report on the General Health Questionnaire (GHQ-12)
|
baseline, 6 months post baseline
|
|
Change in resilience
時間枠：baseline, 6 months post baseline
|
Self report on the Resilience Scale (RS-14)
|
baseline, 6 months post baseline
|
|
Change in perceived employment obstacles
時間枠：baseline, 6 months post baseline
|
Self-report on the Perceived Employment Barriers Scale (PEBS-20)
|
baseline, 6 months post baseline
|
|
Change in perceived employment hope
時間枠：baseline, 6 months post baseline
|
Self-report on the Employment Hope Scale (EHS-14)
|
baseline, 6 months post baseline
|
協力者と研究者
スポンサー
捜査官
- 主任研究者：Mikaela Starke, PhD、Department of Social Work, Gothenburg University
研究記録日
主要日程の研究
研究開始 (予想される)
一次修了 (予想される)
研究の完了 (予想される)
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?
IPD プランの説明
IPD 共有時間枠
IPD 共有アクセス基準
IPD 共有サポート情報タイプ
- STUDY_PROTOCOL
- SAP
- ICF
- CSR
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
米国FDA規制機器製品の研究
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。