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Study identifier: NCT06807060 Synced from ClinicalTrials.gov · August 09, 2026
● Study status: Recruiting

A Municipality Implemented Behavioural Intervention to Improve Quality of Life Among Older Adults

Condition: Quality of Life  ·  Sponsor: Lund University

PhaseNA
Planned participants40
Who can joinAll sexes, 70 Years to no upper limit
Healthy volunteersYesCheck eligibility criteria ↓
Where4 locations

Interested? Contact the study team ↓

For sponsors, CROs & site teams
Professional view of this study — listed sites, countries and recruiting context from the public registry. Everything below is written for patients and caregivers.See where this study is running →

About this study

Ageing is associated with circadian rhythm sleep disorders, poor sleep at night, less physical activity and more time spent indoors, affecting the wellbeing of older adults. Their sleep and mood could benefit from daytime outdoor physical activity, exposure to daylight, better indoor lighting and sleep routines. However, maintaining or increasing one's physical activity can be challenging depending on individual behavioural conditions, e.g., having the physical and cognitive capacity (capability), finding the activity enjoyable and relevant to one's needs (motivation), and having a supportive social and physical environment (opportunity), such as a walk-friendly environment. To address these challenges, a complex behavioural intervention was developed. The intervention is delivered as a web-based course ('Light, activity and sleep in my daily life', LAS) that targets light-related behaviour, outdoor walking and sleep behaviour among community-dwelling older adults. This protocol describes a pilot case study aiming to evaluate the usability and usefulness of the LAS intervention, the intervention outcomes and whether changes to routines are sustained. Eligible intervention participants (target N=40) are Swedish-speaking adults (≥ 70 years), living in one-person households in apartments in four municipalities. Participants complete questionnaires assessing intervention outcome measures (e.g., quality of life), are interviewed about their daily routines, and wear an acceleromet…

This description comes directly from the study's public registry record.

Talk to the study team

Kiran M Gerhardsson, PhD  ·  +46 767 23 27 56  ·  kiran.maini_gerhardsson@med.lu.se

Steven M Schmidt, PhD  ·  steven.schmidt@med.lu.se

There is no obligation to join — the study team can answer your questions about taking part.

Always discuss trial participation with your own doctor first.

Full eligibility criteria (exactly as the study team wrote them)

Inclusion Criteria: * aged 70 and over, ambulatory and sighted, * Swedish speaking, * living independently in one-person households in ordinary apartments and * receiving no or limited home care services. Exclusion Criteria: Study participants will be excluded if they have any condition that makes it difficult to participate.

Reproduced word-for-word from the public registry record — the study team can answer questions about it.

Locations (4)

Gothenburg MunicipalityGothenburg, SwedenRecruiting
Jönköping MunicipalityJönköping, SwedenNot Yet Recruiting
Lund MunicipalityLund, SwedenActive Not Recruiting
Malmö MunicipalityMalmö, SwedenActive Not Recruiting

More studies in these areas

This study lists sites in the areas below. Each link shows other recruiting studies near that city, from the public registry record.

GothenburgJönköpingLundMalmö

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