SHINE - social prescribing for adults and the elderly: the path to effective implementation. A study protocol.
Jeanette Wassar Kirk, Lisa Suvarna Oldrup, Mette Bendtz Lindstrøm...
https://pubmed.ncbi.nlm.nih.gov/41088466Actively Recruiting
Led by Hvidovre University Hospital · Updated on 2025-07-24
350
Participants Needed
1
Research Sites
N/A
Total Duration
H
Hvidovre University Hospital
Lead Sponsor
V
Volunteer Center Sydhavnen
Collaborating Sponsor
Social Prescribing (SP), known as Social Henvisning (SH) in Denmark, connects healthcare with social and cultural services to address factors influencing health beyond medical care. The 'Social Prescribing Vesterbro-Sydhavnen' initiative, starting in fall 2024, involves general practitioners (GPs) referring patients to social services through a dedicated link worker. This evaluation assesses how this project affects healthcare use, loneliness, and quality of life as part of the SHINE Implementation Research Programme. The SP intervention includes various steps such as GP referrals, link worker contacts, personalized service matching, care coordination, visits to local services, accompanied support if needed, and group courses. The intervention is delivered through these pathways, with follow-up and re-prescribing as appropriate. Participants are adults referred by their GPs to receive this support starting in summer 2025. Participants engage by meeting the link worker who explains the evaluation and collects informed consent. Patient reported outcomes on loneliness and health-related quality of life are collected at baseline, 3 months, and 9 months via questionnaires, with reminders sent by SMS or email. Healthcare use data are analyzed from registries. The study measures changes in GP contacts, hospital visits, emergency calls, loneliness scores, and quality of life, with safety and data privacy ensured throughout. The total participation spans at least 9 months post referral.
CONDITIONS
Effectiveness Evaluation of Social Prescribing
You may qualify if you...
You will not qualify if you...
History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety
Complete this quick 3-step screening to check your eligibility
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 screening and enrollment visit (in-person) with the link worker where the study is explained and consent is obtained
Duration - Up to 9 months
Participants engage in the Social Prescribing intervention which involves personalized support from their GP and a link worker to address social and health needs through community services.
Initial meeting with the link worker followed by periodic follow-up contacts and consultations as needed; questionnaires completed at baseline, 3 months, and 9 months
Total: 1 location
1
Volunteer Center Sydhavnen
Copenhagen, Denmark, 2450
Actively Recruiting
M
Mette B Lindstroem, MPH
O
Ove Andersen, Professor, MD
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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Jeanette Wassar Kirk, Lisa Suvarna Oldrup, Mette Bendtz Lindstrøm...
https://pubmed.ncbi.nlm.nih.gov/41088466