CClinicalTrials.gg
Not yet recruitingNCT05950373Updated Apr 3, 2024

Educational Intervention for Better Nutrition to Preserve Functionality - Design of a Randomised Clinical Trial

An interventional study of Education video in Malnutrition, sponsored by Nord University. Not yet recruiting at 1 site in Norway. Open to participants aged 65 Years to 110 Years. Per ClinicalTrials.gov, last updated 2024-04-03.

Sponsored by Nord University · Not applicable, Interventional, and Prevention

From the registry’s dates

  • Primary completion was expected by Nov 2025, 10 months ago, but the record still lists the study as not yet recruiting.
Phase
Not applicable
Study type
Interventional
Enrollment
276
Allocation
Randomized
Ages
65 Years to 110 Years
Sex
All
01

Study summary

This project explores whether access to a digital education video can improve the nutritional situation of home-living older adults after being discharged from the hospital.

02

Conditions studied

  • Malnutrition

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Keywords

  • Older adults
  • Diseases-related malnutrition
  • Educational video
03

In context

Malnutrition

1,588 studies on the registry are indexed under Malnutrition; 237 are open to participants now.

This study's planned enrollment of 276 is above the median of 90 across 1,135 interventional studies indexed under Malnutrition.

Browse Malnutrition studies →

Lead sponsor

Nord University is the lead sponsor of 4 studies on the registry; 2 are open to participants now.

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

04

Who can participate

Ages eligible
65 Years to 110 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Surgical patients embedded in a regional hospital.
  • Home-living in one of nine selected municipalities.
  • Be able to read and understand Norwegian.
  • Have a consent competence.
  • Have a body mass index \< 24.
  • Have access to a digital solution such as a tablet or phone.

Exclusion criteria

Exclusion Criteria:

  • Persons given only a liquid diet.
  • Persons in a terminally ill phase.
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Triple (Care provider, Investigator, Outcomes assessor)
Enrollment
276 participants (estimated)

Study arms

  • Experimental
    Intervention group

    The Intervention group will get access to a six-minute long education video five days after being discharges from the hospital. The video is focusing on protein and energy meals for older adults. The educational film is available via a link on a tablet/ computer or mobile phone. The education video vil only be given one time.

    Other: Education video

  • No intervention
    Control group

    The control group will not be given any intervention.

Interventions

  • OtherEducation video

    six minute long education video focusing on protein and energy meals for older adults.

06

What researchers measure

Primary outcomes

  1. Health related quality of life Using Rand 36 questionaire

    Using Rand 36 questionaire. The data from the SF-36 ordinal subscales will be transformed to a ratio scale using the syntax SF-36 manual and will be presented as the results from each of the eight subscales and the two main scales

    Time frame: Change in Health related quality of life Using Rand 36 questionaire after 3 months

Secondary outcomes

  1. Body fat

    Body fat will be measured by Body mass index (BMI). Weight (in kg) and height (in cm) will be combined to report BMI in Kg/m2

    Time frame: Change in Body mass index after 3 months.

  2. Readmissions to hospital after discharge from the hospital

    Readmissions after discharge from the hospital will be measured three months after discharge.

    Time frame: Registration of Readmissions 3 months after

  3. Muscle strength

    Measure Muscle Strength (in Kg) using Hydraulic Hand dynameter for Hand Grip strength in both hands.

    Time frame: Change in Hand Grip Strength (muscle strength) after 3 months

  4. The mid-arm circumferences

    The mid-arm circumferences (MAC) will be measured in cm with a measuring tape. This will be done on the left upper arm measured at the midpoint between the top of the shoulder and the tip of the elbow.

    Time frame: Change in the mid-arm cirumferences after three months.

  5. Subcutaneous fat

    Subcutaneous fat will be measured by Triceps skinfold thickness (TFS). This will be done in millimetres with a VirtuFits Digital Fat caliper skinfold in the triceps of the left arm.

    Time frame: Change in Subcutaneous fat after three months.

  6. Muscle protein mass

    Muscle protein mass will be measured by the mean arm muscle circumferences (MAMC) calculated to the formula: MAMC (cm) = MAC (cm) - (3,14 X TFS X 0,1)

    Time frame: Change in Muscle protein mass after 3 months

  7. Knowledge about nutrition

    Participants' knowledge about nutrition will be measured with a questionaire consisting of three questions related to the education video.

    Time frame: Registration in a questionaire three months after discharge from the hospital.

07

Study locations

1 site
  • Monica Christin Hansen
    Bodø, 8020, Norway
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 3, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05950373
Lead sponsor
Nord University
Responsible party
Monica Christin Hansen (PhD student, Nord University) — Principal investigator
First posted
Jul 18, 2023
Start date
Jan 1, 2025 (estimated)
Primary completion
Nov 30, 2025 (estimated)
Completion
Oct 1, 2026 (estimated)
Last update
Apr 3, 2024

Study contacts

Monica Hansen, Master
Contact
monica.c.hansen@nord.no
0047 75517250

Oversight

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

Not currently enrolling

This study is not yet recruiting, as verified in Apr 2024. You cannot join it, but the record below documents what was studied.

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