A program to reduce loneliness in older adults in Sweden
Social Prescribing in Sweden (SPiS)- An Interventional Research Project Evaluating a Swedish Model
This study is testing a new program in Sweden that helps older adults who feel lonely connect with community activities to see if it can make them feel better and less isolated.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 220 (estimated) |
| Ages | 65 Years and up |
| Sex | All |
| Sponsor | Umeå University Academic / other |
| Locations | 1 site (Umeå) |
| Trial ID | NCT04336553 on ClinicalTrials.gov |
What this trial studies
This project aims to address the pressing issue of loneliness among older adults in Sweden by implementing a social prescribing program inspired by a successful initiative in the United Kingdom. The program involves General Practitioners referring older adults experiencing loneliness to a coordinator who helps them engage in community activities tailored to their needs. The study will develop and evaluate this Swedish version of social prescribing, focusing on its effectiveness in reducing loneliness and improving overall wellbeing. By collaborating with researchers, healthcare providers, and community stakeholders, the project seeks to create a sustainable model for enhancing social participation among older adults.
Who should consider this trial
Good fit: Ideal candidates for this program are individuals aged 65 and older who are experiencing feelings of loneliness.
Not a fit: Patients with cognitive impairments who cannot provide informed consent will not benefit from this program.
Why it matters
Potential benefit: If successful, this program could significantly reduce loneliness and improve the health and wellbeing of older adults in Sweden.
How similar studies have performed: While social prescribing has shown promise in the UK, this specific approach in Sweden is novel and has not been previously tested.
Eligibility criteria
Show full inclusion / exclusion criteria
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
Where this trial is running
Umeå
- Hälsocentralen Husläkarna — Umeå, Sweden (Recruiting)
Study contacts
- Principal investigator: Ingeborg Nilsson — Umeå University
- Study coordinator: Frida Jonsson, PhD
- Email: frida.jonsson@umu.se
- Phone: +46907869597
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.