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Pathways to Employment for the Long-term Unemployed

23. juli 2020 opdateret af: Göteborg University

Pathways to the Labor Market for Long-term Unemployed: a Comparison of Labor Market Interventions Effects Mechanisms and Implementation

This project's aims are twofold (1) to uncover and define the underlying theories of change guiding competing active labor market programs (ALMP) in Sweden, and (2) to assess the relative effectiveness of these competing programs in a theory-based non-randomized controlled trial. The purpose is to assess the extent to which competing ALMPs are effective in moving long-term unemployed individuals (i.e. unemployed for 6 months or more) closer to the labor-market.

Studieoversigt

Status

Ukendt

Betingelser

Detaljeret beskrivelse

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.

Undersøgelsestype

Observationel

Tilmelding (Forventet)

200

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

18 år til 65 år (Voksen, Ældre voksen)

Tager imod sunde frivillige

Ingen

Køn, der er berettiget til at studere

Alle

Prøveudtagningsmetode

Ikke-sandsynlighedsprøve

Studiebefolkning

All individuals receiving intervention from participating service providers during the inclusion period that meet the inclusion criteria.

Beskrivelse

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

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

Kohorter og interventioner

Gruppe / kohorte
Intervention / Behandling
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

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Change in employment and earnings
Tidsramme: baseline, 6 months post baseline
Employment and earnings data collected from official register data
baseline, 6 months post baseline

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Change in general health
Tidsramme: baseline, 6 months post baseline
Self report on the General Health Questionnaire (GHQ-12)
baseline, 6 months post baseline
Change in resilience
Tidsramme: baseline, 6 months post baseline
Self report on the Resilience Scale (RS-14)
baseline, 6 months post baseline
Change in perceived employment obstacles
Tidsramme: 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
Tidsramme: baseline, 6 months post baseline
Self-report on the Employment Hope Scale (EHS-14)
baseline, 6 months post baseline

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Efterforskere

  • Ledende efterforsker: Mikaela Starke, PhD, Department of Social Work, Gothenburg University

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Forventet)

1. september 2020

Primær færdiggørelse (Forventet)

1. juni 2021

Studieafslutning (Forventet)

1. december 2021

Datoer for studieregistrering

Først indsendt

27. januar 2020

Først indsendt, der opfyldte QC-kriterier

28. januar 2020

Først opslået (Faktiske)

30. januar 2020

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

24. juli 2020

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

23. juli 2020

Sidst verificeret

1. juli 2020

Mere information

Begreber relateret til denne undersøgelse

Andre undersøgelses-id-numre

  • 2018-01324

Plan for individuelle deltagerdata (IPD)

Planlægger du at dele individuelle deltagerdata (IPD)?

JA

IPD-planbeskrivelse

De-identified participant data for primary and secondary outcome measures will be made available.

IPD-delingstidsramme

Data will be made available within 6 months of study completion

IPD-delingsadgangskriterier

Data access requests will be reviewed and must be accompanied by an ethical approval to use data.

IPD-deling Understøttende informationstype

  • STUDY_PROTOCOL
  • SAP
  • ICF
  • CSR

Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter

Studerer et amerikansk FDA-reguleret lægemiddelprodukt

Ingen

Studerer et amerikansk FDA-reguleret enhedsprodukt

Ingen

Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .

Abonner