Strength for Caregiving

NCT07615205 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 100

Last updated 2026-05-29

No results posted yet for this study

Summary

The goal of this single-arm pre-post study is to promote elderly (≥ 65 years) family caregivers' dietary habits, well-being and functional capacity through comprehensive nutritional guidance. The main goals of the project are to:

* Improve the well-being, resilience, and functional capacity of the participating family caregivers through the comprehensive nutritional counseling implemented as part of the project.
* Create a nutrition counseling model that promotes the well-being and coping of family caregivers and can also be utilized in well-being services counties after the project concludes.
* Produce up-to-date and practical nutrition materials for family caregivers.

The project participants will participate in two individual nutrition counselling sessions and three group nutrition counseling sessions over a period of ten months.

Researchers will compare the results of the participants' baseline and final measurements to see if nutrition counseling is effective in improving family caregivers' well-being, resilience, and functional capacity.

Conditions

  • Mental Well-being
  • Muscle Strengh
  • Dietary Habits
  • Quality of Life
  • Nutritional Status
  • Functional Capacity

Interventions

BEHAVIORAL

Tailored nutritional counselling intervention

The intervention is a 10-month tailored nutritional counselling programme for elderly family caregivers. It includes two individual dietary counselling sessions conducted by a nutrition specialist and three group counselling sessions. The individual counselling sessions include a personal nutrition plan based on the participant's needs. According to participants' preferences, the group counselling sessions consist of either nutrition lectures or practical cooking courses. The intervention aims to improve participants' well-being, functional capacity, and dietary habits.

Sponsors & Collaborators

  • City of Pori

    collaborator UNKNOWN
  • City of Rauma

    collaborator UNKNOWN
  • The Martha association of South West Finland

    collaborator UNKNOWN
  • City of Kankaapää

    collaborator UNKNOWN
  • Satakunta Wellbeing Services County

    collaborator UNKNOWN
  • Adult education centre of Pori

    collaborator UNKNOWN
  • Adult education centre of Rauma

    collaborator UNKNOWN
  • Petäjä Adult Education Centre

    collaborator UNKNOWN
  • Susanna Kunvik

    lead OTHER

Principal Investigators

  • Susanna Kunvik · Satakunta University of Applied Sciences

Study Design

Allocation
NA
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
65 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2026-09-30
Primary Completion
2027-11-30
Completion
2027-11-30

Countries

  • Finland

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07615205 on ClinicalTrials.gov