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RecruitingNCT07545915Updated Apr 22, 2026

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

An interventional study of Health Web Te@m in Healthy Older Adults, sponsored by Luleå Tekniska Universitet. Recruiting at 1 site in Sweden. Open to participants aged 65 Years and older. Per ClinicalTrials.gov, last updated 2026-04-22.

Sponsored by Luleå Tekniska Universitet · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 5 months after the study started (first participant enrolled Nov 2025, registered Apr 2026).
  • Started Nov 2025; still recruiting 11 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
27
Allocation
Not applicable
Ages
65 Years and older
Sex
All
01

Study 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.
Read the 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.

02

Conditions studied

  • Healthy Older Adults

Keywords

  • complex interventions
  • healthy ageing
  • older adults
  • interprofessional team
  • meaningful activity
  • digitalization
  • group intervention
03

In context

Lead sponsor

Luleå Tekniska Universitet is the lead sponsor of 13 studies on the registry; 4 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
65 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

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

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
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
27 participants (estimated)

Study arms

  • Experimental
    The older adults will receive the Health Web Te@m intervention provided by an interprofessional team

    Behavioral: Health Web Te@m

Interventions

  • BehavioralHealth 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 become aware of, reflect on, use and develop strategies for healthy ageing.

06

What researchers measure

Primary outcomes

  1. The Swedish RAND-36 Health Survey

    RAND-36 comprises 35 items covering eight health dimensions: physical functioning, role limitations due to physical health, role limitations due to emotional problems, social functioning, mental well-being, vitality, pain, and general health. Also including a global item assessing perceived health change over the past 12 months. The time intervals vary for different questions: In general, compared to a year ago, current health (a typical day), and the last 4 weeks. The respondent rates the degree of discomfort within the different dimensions on a scale with three, four, five, or six response options, with the exception of two questions that are answered with yes or no.

    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 outcomes

  1. Occupational Balance Questionaire (OBQ)

    The OBQ consists of 11 items that are graded on a 4-point ordinal scale from 0-3; these items range from "completely" disagree to "completely" agree and are summed to a total score ranging between 0 and 33. A higher score implies more satisfaction with the amount and variation of occupations, i.e., a higher level of occupational balance. Used to capture the satisfaction with, and the variation in daily activities.

    Time frame: Within 2 weeks before the intervention is initiated and within 2 weeks after the intervention is completed

  2. The general self-efficacy scale (S-GSE)

    Each item consists of a statement about one's ability to cope with demands in life. The participant rates each item on a scale from 1-4, where 1 represents "disagree" and 4 represents "strongly agree" with the statement; thus, a higher score (total score 10-40) indicates greater self-efficacy. Used to measure self-perceived self-efficacy

    Time frame: Within 2 weeks before the intervention is initiated and within 2 weeks after the intervention is completed

  3. UCLA Loneliness scale

    Perceived loneliness will be assessed using the UCLA Loneliness scale which is a 20-item scale that assesses three dimensions of loneliness: emotional loneliness, social loneliness, and existential loneliness. Each item is rated on a 4-point Likert scale (ranging from 1, "never," to 4, "often") and the total score can range from 20 to 80, with higher scores indicating greater feelings of loneliness.

    Time frame: Within 2 weeks before the intervention is initiated and within 2 weeks after the intervention is completed

  4. The Swedish version of UAB Study of Aging Life-Space Assessment (LSA-S)

    LSA-S evaluates an individual's mobility within their environment by assessing levels of movement, frequency of mobility, and the degree of assistance required. The instrument maps movement patterns across five defined "life-space" levels. For each level, frequency and independence are recorded, generating a quantitative total score ranging from 0 to 120.The score for each level is calculated by multiplying the level (1-5) by a frequency factor (1-4) and a factor representing the degree of independence.

    Time frame: Within 2 weeks before the intervention is initiated and within 2 weeks after the intervention is completed

  5. Intervention-specific registration forms for older adults

    These registration forms contain questions about content and delivery for which answers are self-reported on a 5-point Likert scale ranging from very low agreement (1) to very high agreement (5). Older adults will score their level of agreement as follows: a) gain of new and useful knowledge, b) value of reflection assignments, c) value of and engagement in group discussions, and d) use of the digital communication platform. Space is also provided in the registration form to write their own comments.

    Time frame: Completed by older adults within 1 week after each theme session 1-6

  6. Intervention-specific registration forms for professionals

    These registration forms contain questions about delivery for which answers are self-reported on a 5-point Likert scale ranging from very low agreement (1) to very high agreement (5). The professionals will score their level of agreement with the following: a) compliance with the intervention guide, b) achieving the purpose of the session, c) perceived support from the intervention guide, d) confidence in the role as a group leader, e) satisfactory management of the digital communication platform and f) satisfactory management of the digital communication platform by older adults. Space is also provided in the registration form to write their own comments.

    Time frame: Completed by the professionals within 1 week after each theme session 1-6

  7. Individual semi-structured interviews with older adults

    The pre-intervention questions aim to capture their current everyday activities, what they find meaningful and how they experience their health. Further, their motivators for participation and their expectations of participation in the intervention. Directly after the programme is completed, the interviews will explore experiences of the different parts of the intervention process and the perceived value of the intervention for their everyday activities, social participation and health.

    Time frame: Within 2 weeks before the intervention is initiated and within 2 weeks after the intervention is completed

  8. Group interviews with the interprofessional teams

    The questions for the group interview before delivery will explore the interest in and motivation to deliver the intervention, expectations of conducting a digital intervention and their role as a group leader. In the group interviews after, the questions will explore experiences of delivering the intervention, compliance with the intervention guide, experiences of their role as a group leader, the digital delivery and time used, and the relevance of the content and the overall value of the intervention. Also, how the education programme prepared them for the delivery of the intervention.

    Time frame: Within 2 weeks before the intervention is initiated and within 2 weeks after the intervention is completed

07

Study locations

1 of 1 sites recruiting
  • Luleå University of Technology
    Luleå, 97187, Sweden
    Recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 22, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07545915
Lead sponsor
Luleå Tekniska Universitet
Responsible party
Anneli Nyman (Professor, Luleå Tekniska Universitet) — Principal investigator
First posted
Apr 22, 2026
Start date
Nov 3, 2025
Primary completion
Dec 2026 (estimated)
Completion
Dec 2026 (estimated)
Last update
Apr 22, 2026

Study contacts

Anneli Nyman, Professor
Contact
anneli.nyman@ltu.se
+460920493888
Elin Hellman, PhD student
Contact
elin.hellman@ltu.se
+460920493648
Anneli Nyman
principal investigator · Luleå Tekniska Universitet

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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