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Effects of Whey and Collagen on FFM, Muscle Strength and Wound Healing in Elderly Surgical Patients

The Effects of Whey Protein and Collagen on Fat Free Mass, Muscle Strength and Wound Healing in Elderly Patients Undergoing Elective Knee- or Hip Surgery

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04496856
Enrollment
15
Registered
2020-08-03
Start date
2020-05-10
Completion date
2020-12-30
Last updated
2021-09-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hip Arthritis, Knee Arthritis, Sarcopenia

Keywords

Hip Arthroplasty, Collagen, Whey protein, Knee Arthroplasty

Brief summary

The purpose of the study is to compare the effect of whey protein and collagen on fat free mass, muscle strength, functional ability, wound healing and life quality in elderly patients undergoing elective knee- or hip surgery (defined as elective knee- or hip arthroplasty). The patients are admitted at the department of Orthopaedic Surgery at Herlev Gentofte Hospital.

Interventions

DIETARY_SUPPLEMENTWhey protein and Collagen supplementation

Participants of each arm will consume 30 g daily of the assigned protein supplementation for 30 days. The protein supplementation will be given as protein powder which the participants will have to dissolve in cold drinks. During the intervention fat free mass, muscle strength, functional ability, wound healing and life quality of the participants will be monitored.

Sponsors

Herlev and Gentofte Hospital
CollaboratorOTHER
University of Copenhagen
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age 65+ years * Scheduled elective knee- or hip surgery * Must be able to understand and speak danish * Must be able to chew and swallow food with a regular consistency * Must be able to consume the assigned protein supplementation * Must be able to consent participation

Exclusion criteria

* Vegan * Demensia * Critical complications to the surgery which prevents the patient from participating in the rehabilitation program * Plasma-creatinin above 250 micromol/L * Palliative patients * Known intolerance of whey protein and/or collagen * Patients with a pacemaker

Design outcomes

Primary

MeasureTime frameDescription
The difference in fat free massWeekly for 30 daysThe outcome will be monitored through BIA and the development of fat free mass in the operated leg will be compared to the development of fat free mass in the non-operated leg.

Secondary

MeasureTime frameDescription
Handgrip strengthWeekly for 30 daysHandgrip strength measured by a handdynanometer (SAEHAN) in kg and percentage
Extension strength of quadriceps femorisWeekly for 30 daysMeasured in amounts of repetitions of 0.5 or 1.0 kg.
Life qualityWeekly for 30 daysMeasured trough EuroQol-5D-5L
Difference in functional ability (NMS)Weekly 30 daysAssessed by New mobility score
Difference in Chair stand testWeekly for 30 daysMeasured by amount of repetitions
Wound healingWeekly for 30 daysThe amount of days until the wound is healed (defined as: the epithelium is covered without crust). This will be monitored trough pictures and assessed on a scale from 1-5 by a masked doctor.
Redness and infectionWeekly for 30 daysThe redness and infection around the wound assessed on a scale from 1-5 by a masked doctor through pictures.

Other

MeasureTime frameDescription
Compliance of the protein supplementation intakeWeekly for 30 daysAssessed trough a weekly form, which the participants will fill in
Rapported side effects30 daysParticipants will be informed to rapport if they experience any side effects throughout the intervention
Palatability of the protein supplementation30 daysAssessed on a scale from 1-5
Consistency of the protein supplementation30 daysAssessed on a scale from 1-5

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026