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Long Term Social Assistance Recipient in South Eastern Sweden - a Description of Health, Function, and Activity

21 de noviembre de 2018 actualizado por: Bjorn Gerdle, Linkoeping University

Long Term Social Assistance Receipt - An Observational Study of Health, Function, and Activity

There is a group of social assistance recipients which have difficulties in entering the labor market and thus remains in a long-term dependency on social assistance. More knowledge about individuals receiving long-term social assistance is needed in order to improve into work interventions for this group. Therefore, this study aims to describe variables of health, function and activity in participants receiving long-term social assistance.

Descripción general del estudio

Estado

Desconocido

Descripción detallada

There is a group of social assistance recipients who have difficulties in entering the labor market and thus remains in a long-term dependency on social assistance. More knowledge about individuals receiving long-term social assistance is needed in order to improve into-work interventions for this group. Therefore, this study aims to describe variables of health, function and activity in participants receiving long-term social assistance. Individuals who have received social assistance during more than three years, who report physical and/or psychological difficulties, and/or have a complex social situation will be asked for participation in a six months activity-based investigation including contact with social worker, psychologist, occupational therapist, physical therapist and labor market consultant. The intervention aims to clarify the participants hinders and resources for entering the labor market. The participants are going to answer a questionnaire about health, function, and activity before and after the investigation. In addition, the participants function and ability to perform activities will be classified using the International Classification of Functioning (ICF). Data from the questionnaires and from ICF recordings will be used to describe variables of health, function and ability to be active. Participants who manage to get closer to, or enter into, the labor market will be asked to participate in a qualitative interview study about the experiences of the change. In addition, social workers will be asked to participate in focus-group interviews about experiences from the professional contact and work with the participants. The quantitative data will be analysed using traditional statistics and multivariate data analysis. Qualitative data will be analysed using qualitative content analysis.

Tipo de estudio

De observación

Inscripción (Anticipado)

100

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Estudio Contacto

Ubicaciones de estudio

    • Östergötland
      • Linköping, Östergötland, Suecia, SE 581 85
        • Faculty of Health Sciences, Linköping University

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

18 años a 65 años (Adulto, Adulto Mayor)

Acepta Voluntarios Saludables

No

Géneros elegibles para el estudio

Todos

Método de muestreo

Muestra no probabilística

Población de estudio

Individuals who have been social assistance recipients for at least three years and who not have a plan how to get closer to the labor market. There may be signs of different kinds of ill-health such as physical, pshychological and/or social ill-health. The social worker responsible for decision about the monetary support identifies a need for establishing the working ability of the individual with the aim to agree on a plan towards self-sufficiency.

Descripción

Inclusion Criteria:

  • Long-term social assistance recipient (more than three years)
  • Putative ill-health (physical, psychological and/or social)
  • No present plan how to reach the labor market
  • Need of clarifying the working ability

Exclusion Criteria:

  • Homelessness
  • Severe psychiatric illness
  • Abuse of alcohol or substances

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

Cohortes e Intervenciones

Grupo / Cohorte
Intervención / Tratamiento
Health and activity
The cohort consists of long-term social assistance recipients where there is need to investigate the health status and working ability.
During a six months multidisciplinary investigation of health status, activity and working ability for individuals receiving long-term social assistance, the health and activity status as well as function will be described using established questionnaires and the International Classification of Functioning

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Change in quality of life
Periodo de tiempo: Change between the beginning and the end of the six months intervention
The change in participants self-rated experience of quality of life is going to be described using EuroQol 5 Dimensions which contains a rating of the ability to perform activities, and also a score of the total quality of life experience.
Change between the beginning and the end of the six months intervention
Change in self-rated function and ability to be active
Periodo de tiempo: Change between the beginning and the end of the six months intervention
The change in participants self-rated function and ability to be active is going to be described using the World Health Organisation Disability Assessment Schedule (WHODAS) which contains five-grade ratings of factors including functioning, activity and participation.
Change between the beginning and the end of the six months intervention
Change in objective description of function and ability to be active
Periodo de tiempo: Change between the beginning and the end of the six months intervention
The change in an objective classification of function, activity, participation and environmental factors affecting disability will be described according to the International Classification of Functioning (ICF) in the beginning and at the end of the six month intervention. The ICF contains a number of components, where each component can be scored using a five-grade scale to clarify the magnitude of disability.
Change between the beginning and the end of the six months intervention

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Qualitative description of experiences about an increase in activity ability
Periodo de tiempo: After the six moths intervention
Participants experiences about a change towards higher ability to be active will be described using qualitative interviews.
After the six moths intervention
Qualitative description of social workers experiences from the work with long-term social assistance recipients
Periodo de tiempo: After the six moths intervention
Social workers experiences from their work with helping clients to get closer to the labor market will be described using qualitative interviews.
After the six moths intervention

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Patrocinador

Colaboradores

Investigadores

  • Silla de estudio: Linn Karlsson, PhD, Linkoeping Municipality, Linkoeping University

Publicaciones y enlaces útiles

La persona responsable de ingresar información sobre el estudio proporciona voluntariamente estas publicaciones. Estos pueden ser sobre cualquier cosa relacionada con el estudio.

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Anticipado)

1 de diciembre de 2018

Finalización primaria (Anticipado)

1 de enero de 2021

Finalización del estudio (Anticipado)

1 de enero de 2021

Fechas de registro del estudio

Enviado por primera vez

19 de noviembre de 2018

Primero enviado que cumplió con los criterios de control de calidad

21 de noviembre de 2018

Publicado por primera vez (Actual)

23 de noviembre de 2018

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

23 de noviembre de 2018

Última actualización enviada que cumplió con los criterios de control de calidad

21 de noviembre de 2018

Última verificación

1 de noviembre de 2018

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • TU-001-1811

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

Descripción del plan IPD

The co-authors will have access to the underlying interview data for the qualitative analysis. Quantitative data will be coded and not able to identify to any participant for the co-authors. However, it may be necessary for the co-authors to get access to the quantitative (anonymized) raw data.

Marco de tiempo para compartir IPD

The data will become available during analysis and manuscript writing. Probable for about six moths per paper.

Criterios de acceso compartido de IPD

Co-authors who will be participating in analysis and manuscript preparation.

Tipo de información de apoyo para compartir IPD

  • PROTOCOLO DE ESTUDIO
  • SAVIA
  • CIF
  • CÓDIGO_ANALÍTICO
  • RSC

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

Ensayos clínicos sobre Investigation of health and activity

3
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