Health Web Te@m (1.0) an Interprofessional Web-based Group Intervention Supporting Healthy Ageing (NCT07545915) | Clinical Trial Compass
RecruitingNot Applicable
Health Web Te@m (1.0) an Interprofessional Web-based Group Intervention Supporting Healthy Ageing
Sweden27 participantsStarted 2025-11-03
Plain-language summary
The goal of this study is to evaluate the feasibility of Health Web - Te@m 1.0 for older adults in selected primary healthcare settings in northern Sweden. More specifically, the feasibility will be assessed through the following objectives:
* Explore older adults' experiences of the intervention process, acceptability, and perceptions of the value of participating in Health Web - Te@m.
* Explore professionals' experiences of acceptability, value, and implementation potential of delivering Health Web - Te@m in primary healthcare settings.
* Evaluate adherence to Health Web - Te@m among older adults and professionals.
* Evaluate the assessments' ability to detect potential outcomes of Health Web - Te@m.
Who can participate
Age range
65 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* 65 years or older and retired
* live in ordinary housing
* experience a changed life situation that can pose a risk of reduced social participation and health
* have access to a computer or tablet, access to and experience of using the Internet and e-mail
* able to express themselves in speech and assimilate information
Exclusion Criteria:
* have an ongoing application to nursing home
* disease or conditions that affect the ability to provide informed consent and participate in data collection and the intervention
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
The Swedish RAND-36 Health Survey
Timeframe: The outcome measure is completed within 2 weeks before the intervention is initiated and within 2 weeks after the intervention is completed