Social Prescribing in Sweden (SPiS) (SPiS)

May 10, 2023 updated by: Ingeborg Nilsson, Umeå University

Social Prescribing in Sweden (SPiS)- An Interventional Research Project Evaluating a Swedish Model

Loneliness among older adults has become an issue of public concern, as it is associated with increased morbidity and mortality. Yet, despite the urgency, there is little information on how to reduce or prevent loneliness. The focus of this project is using experiences from the United Kingdom's initiative social prescribing, which gives General Practitioners the option of referring clients in need to a coordinator, who in dialogue with the client finds activities for the client to engage in within the local community. Until now, social prescribing has not been tested in Sweden. Therefore, with the overarching goal of reducing loneliness and improving health and wellbeing, the aim of the project is to develop and test a Swedish social prescribing program in order to explore circumstances under which the program can reduce loneliness and improve wellbeing in older adults. The project will be carried out in collaboration between researchers, a primary healthcare center, and a community activity initiative. In the first phase, the research group will bring potential end-users and stakeholders together in workshops to discuss, develop, and design a Swedish program for social prescribing. Interviews with potential end-users and stakeholders will be carried out to analyze challenges and possibilities with the program. In a second phase, the Swedish program will be implemented to evaluate experiences and the effect of Social prescribing in Sweden regarding loneliness, health, wellbeing among older adults (65 yrs or older) in Sweden. The study will be carried out in a feasibility study and a large-scale RCT study. including both qualitative and quantitative data Based on the results of this study, there will be new knowledge gained concerning if and how social prescribing can be used among older adults in a Swedish context.

Study Overview

Status

Recruiting

Conditions

Intervention / Treatment

Detailed Description

Loneliness among older adults has become an issue of public concern. There seems to be a high and stable prevalence of reported loneliness, with as many as 50% of older adults reporting serious or moderate loneliness. There is also growing evidence on the significant harmful effects of loneliness in older adults . Although the situation is urgent, no specific type of intervention has demonstrated a robust evidence base for reducing loneliness. There are, however, promising initiatives that manage to take the wider context in which the individual lives into account. Initiatives such as Social Prescribing in the United Kingdom identify the individual's needs, and guide them in getting involved with their community, by linking people with local supportive social activities and opportunities. However, such initiatives are sensitive to context, and may not be easily transferred between national contexts. The focus of this project is to develop and implement Social Prescribing in a Swedish context, as this has not yet been done. Our novel contribution to this field is: a) developing a Swedish version of a social prescribing method together with potential end-users and stakeholders; and b) evaluating the first test and implementation of this method. Thus, this project has the potential to develop important knowledge regarding how to prevent and/or reduce an urgent public health issue, loneliness among older adults, in a non-medical way via social prescribing in a Swedish context.

Background and point of departure

Systematic reviews show that social isolation and loneliness among older people is a substantial problem (affecting 7-17% and 40% respectively), and that lack of social inclusion and a feeling of loneliness negatively affects physical and mental health. These issues are especially prevalent in older people with health problems, and are associated with socio-demographic factors (gender) and social factors (e.g., civil status and meaningful social contacts). The research findings call for attention to be given to the provision of services for meeting societal ideals in caring for the older generation, confronting the rising isolation and subjective loneliness which harms individual health and burdens national and global economies.

There might though be protective factors addressing loneliness as research demonstrates the importance of social relations and social engagement in older people's health, well-being, and cognitive health. Strong mortality effects also exist,148 longitudinal studies revealed a 50% mortality reduction in persons with strong social relationships.

Societal services need to be developed that prevent loneliness and support social participation. A social equivalent to the physical activity on prescription is the United Kingdom initiative started in 2002 called social prescribing, which serves as a way of linking patients in primary care with sources of support within their local community. Social prescribing concerns expanding the options available to General Practitioners (GP) by allowing them to forward a client with psychosocial issues to existing meaningful activities in the community that meet these needs. There are no set standards in the procedures of social prescribing, but it gives a GP the option of using a non-medical referral, either as a stand-alone, or together with existing treatments. The sources of support in the community can be either in the volunteer or community sectors. Challenges that have been described include the multiplicity of options and the logistical difficulties although the idea is simple, the implementation is complex. What is essential is that there is a direct referral from primary care, and an identified coordinator who connects the person to local activities that meet their needs and aspirations.

Although no robust evidence, findings report that social prescribing is broadly supportive to reducing demand on primary and secondary care, and has the potential to deliver cost savings, improvements in wellbeing, reduction of mental and physical symptoms, as well as a reduction in social isolation and loneliness. There is, in particular, a need to highlight research questions such as; When, for whom, and how well does social prescribing work, and in addition, what effect does it have?

Social prescribing has not yet been tested in a Swedish context. There are reasons to believe that perceptions will differ somewhat between the two countries, partly as a consequence of their different ways of understanding relations between the citizen and the "proper" provider of healthcare. With a high number of older adults reporting loneliness, and knowing the harmful effects of this situation, initiatives need to be taken. Social prescribing developed and implemented into a Swedish context is such an initiative.

In the first phase, the researchers will develop and design a social prescribing intervention for a Swedish context (SPiS) and in the second phase, the theory will then be tested while the intervention is implemented in a regular primary healthcare center to assess how the program works. Finally, in a third phase, the program theory will be refined based on the prior developed knowledge.

Co-creation together with a feasibility study and a randomized controlled trial will be used in order to understand and reflect design and development of program for social prescribing.

Both quantitative as well as qualitative data will be collected using different methods. In order to understand feasibility and reach power in the statistics, the program will be implemented in at least eight different primary care centers around Sweden. Randomly older adults will be selected to either get Social prescribing within four working days (intervention group) or be on a waiting list (control group) for three months.

Individual interviews

Group interviews will be performed with representatives from our collaborating partners; a) the health care center, b) the involved community-based activity initiative, and c) local and societal representatives for older adults (65 years old or older) in order to gain knowledge about factors important to address loneliness, health and well-being. Questions about the theoretical underpinnings of the model, the practical implementation of the model in the regular day to day practice as well as the fidelity to the prescription will be important topics to address. Social prescribing per se and its potential effective mechanisms, moderating factors, as well as barriers in the procedure will also be discussed with the profession and stakeholders.

In addition, qualitative interviews will be conducted with the participants who have received social prescribing as well as the professionals who deliver the intervention.

Quantitative measures

Quantitative demographic data of the participants (older adults receiving the SPiS), age, gender, education level, diagnosis affecting activity performance and interests, will be collected at baseline and follow-up followed by measurement of loneliness, self-rated health, mapping of social networks and social support.

Data analysis

The quantitative data will generate evidence regarding the expected outcomes of loneliness, health and activity engagement to address the issue of for whom, under which circumstances, and in what respect the intervention is working. Descriptive statistics, as well as parametric and non-parametric statistical analysis will be used to detect changes between groups of older adults in the outcome variables.

Evidence generated through the qualitative work focusing particularly on contextual factors and potential mechanisms will address the issue of what in the intervention is working and why. Data will be analyzed thematically, with grounded theory approaches and/or other relevant qualitative measures.

Study Type

Interventional

Enrollment (Anticipated)

220

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

  • Sweden
      • Umeå, Sweden
        • Recruiting
        • Hälsocentralen Husläkarna

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

61 years and older (Older Adult)

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

- Persons 65 years or older who experience loneliness will be included after given informed consent

Exclusion Criteria:

- Persons who, due to cognitive impairment, are unable to give informed consent will be excluded

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Intervention: Social prescribing in sweden (SPiS)
Patients (older adults experiencing loneliness) at a Health care clinic are invited to an optional additional internal referral for social prescribing (SPiS) within four working days. SPiS is a means of enabling the professionals to refer people to a range of local, non-clinical services. SPiS will involve a variety of activities, tailored to the patients needs and desires) which are typically provided by voluntary and community sector organisations.
Behavioral: Social prescribing in Sweden (SPiS)
Social prescribing in sweden (SPiS)
No Intervention: Control: Social prescribing in sweden (SPiS)
Patients (older adults experiencing loneliness) at a Health care clinic are invited to an optional additional internal referral for social prescribing (SPiS) within three months. SPiS is a means of enabling the professionals to refer people to a range of local, non-clinical services. SPiS will involve a variety of activities, tailored to the patients needs and desires) which are typically provided by voluntary and community sector organisations.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Loneliness
Time Frame: 0, 3 and 12 month
The UCLA loneliness scale used for studying changes in loneliness interventions, using this scale, participants' self-reported experiences of loneliness will be measured. The measurement includes 20 statements, rated on a four-step scale from never to always. The given scores are summarized into a total score, ranging from 20-80. Four levels of loneliness have been identified and preliminarily established, and the measurement has been used on groups of older people, and frequently in intervention studies.
0, 3 and 12 month

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Health
Time Frame: 0, 3 and 12 months
Change in Self-rated general health will be assessed using the visual analogue scale (VAS) from the EQ-5D scale. The VAS is a psychometric response scale which measures subjective characteristics or experiences in a qualitative way. When responding to the VAS item in this project, the respondents specify their level of agreement to the statement "in general how do you experience your health?" by indicating a position along a continuous line between the two end-points, "best possible health and worst possible health".
0, 3 and 12 months
Health
Time Frame: 0, 3 and 12 months
Short Form Health Survey Swedish version (SF-12), will be used to capture the overall change of subjective health status. The SF-12 is a questionnaire covering physical health and mental well-being. SF-12, developed from SF-36, has established validity and reliability for use in older populations, and has a similar responsiveness to change as SF-36
0, 3 and 12 months
Depression
Time Frame: 0, 3 and 12 months
The GDS-15, depression scale is used to identify changes in symptoms of depression in older adults. The GDS consists of 15 self-rated questions that will assess the level of enjoyment, interest social interaction and more among the older adults. In order to screen for symptoms of depression rather than factors associated with aging, the GDS focuses specifically on psychiatric rather than somatic symptoms.
0, 3 and 12 months
MNPS Interest checklist
Time Frame: 0, 3 and 12 months
The checklist is used to identify changes in leisure engagement. The MNPS interest checklist consist of 20 self-rated questions of interest, doing, motivation and well-being from pre-set leisure activities
0, 3 and 12 months
Social network and support
Time Frame: 0, 3 and 12 months
Questions related self-rated experiences of social network and support from social network
0, 3 and 12 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Umeå University

Collaborators

Forte

Investigators

  • Principal Investigator: Ingeborg Nilsson, Umeå University

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Anticipated)

May 1, 2023

Primary Completion (Anticipated)

October 1, 2024

Study Completion (Anticipated)

December 31, 2025

Study Registration Dates

First Submitted

April 2, 2020

First Submitted That Met QC Criteria

April 6, 2020

First Posted (Actual)

April 7, 2020

Study Record Updates

Last Update Posted (Actual)

May 12, 2023

Last Update Submitted That Met QC Criteria

May 10, 2023

Last Verified

May 1, 2023

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • 1:1

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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