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Recruiting NCT07545915

Health Web Te@m (1.0) an Interprofessional Web-based Group Intervention Supporting Healthy Ageing

No phase Interventional Healthy Older Adults

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Health Web Te@m.
Who it may be relevant to
Registry conditions: Healthy Older Adults. Basic parameters: from 65 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Sweden
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Health Web Te@m (1.0) an Interprofessional Web-based Group Intervention Supporting Healthy Ageing: a Study Protocol for a Feasibility Study

Overview

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.

Detailed description

Ageing populations, together with constraints in healthcare workforce capacity, place increasing pressure on health systems, prompting structural and organizational transformations. In this context, there is a growing emphasis on person-centered, integrated care, where health-promoting interventions play a central role. Health is a multidimensional and dynamic concept that encompasses physical, mental, and social well-being, rather than merely the absence of disease. Consequently, healthy ageing requires a holistic and interdisciplinary approach that strengthens older adults' resources across physical, psychological, social, and environmental domains. A central component of these approaches is supporting individuals in maintaining engagement in meaningful everyday activities, as participation in daily life contributes to a sense of purpose, identity, and overall well-being. In response to this need, an interprofessional web-based group intervention was developed, focusing on strategies for healthy ageing and supporting individuals in managing their daily lives in a sustainable and health-promoting way. This feasibility study will be conducted using a pretest and posttest design without a control group to evaluate feasibility and potential results. Qualitative and quantitative data will be collected concurrently in a mixed-method design. The combination of data enables a comprehensive evaluation of feasibility. The intervention Health Web Team 1.0 is a health promoting intervention is targeting older adults 65+ and is delivered by an interprofessional team in selected primary healthcare settings in northern Sweden. This feasibility study provides important information to further evaluate and refine the intervention programme prior to larger-scale testing.

Interventions

  • Behavioral Health Web Te@m
    The Health Web Te@m intervention is delivered by an interprofessional team via a digital communication platform. The intervention starts with an introduction session followed by six theme sessions and ends with a closing session one month after the last theme session. Each theme session includes a short educational video followed by a reflection assignment, and a group meeting moderated by one of the professionals in the interprofessional team. The intervention aims to support older adults to be

Primary outcome measures

  • The Swedish RAND-36 Health Survey [Time frame: The outcome measure is completed within 2 weeks before the intervention is initiated and within 2 weeks after the intervention is completed]
Secondary outcome measures (8)
  • Occupational Balance Questionaire (OBQ) [Time frame: Within 2 weeks before the intervention is initiated and within 2 weeks after the intervention is completed]
  • The general self-efficacy scale (S-GSE) [Time frame: Within 2 weeks before the intervention is initiated and within 2 weeks after the intervention is completed]
  • UCLA Loneliness scale [Time frame: Within 2 weeks before the intervention is initiated and within 2 weeks after the intervention is completed]
  • The Swedish version of UAB Study of Aging Life-Space Assessment (LSA-S) [Time frame: Within 2 weeks before the intervention is initiated and within 2 weeks after the intervention is completed]
  • Intervention-specific registration forms for older adults [Time frame: Completed by older adults within 1 week after each theme session 1-6]
  • Intervention-specific registration forms for professionals [Time frame: Completed by the professionals within 1 week after each theme session 1-6]
  • Individual semi-structured interviews with older adults [Time frame: Within 2 weeks before the intervention is initiated and within 2 weeks after the intervention is completed]
  • Group interviews with the interprofessional teams [Time frame: Within 2 weeks before the intervention is initiated and within 2 weeks after the intervention is completed]

Eligibility criteria

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

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
N/A
Model
Single group
Masking
Open label
Primary purpose
Treatment

Study locations

Sweden · 1 center
  • Luleå University of Technology — Luleå

Identifiers

NCT: NCT07545915 · Health Web Te@m - 633940 · 633316

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗