Clinical Trial Summary
Recruiting will be performed via checking the calendar for scheduled TKA procedures in the >
8 weeks by clinical staff in the UAMS orthopedic clinic. Clinic staff will look for basic
inclusion/exclusion criteria in the EMR for those patients. Clinic staff will either contact
directly or send contact information to the PI of this study to contact for recruitment
purposes. During the initial phone call, study staff will review inclusion/exclusion criteria
to verify eligibility and will discuss study specifics and send a link to the current
informed consent form located on the UAMS REDCap server. If the subject wishes to enroll,
they will do so via electronic consent through REDCap. REDCap will notify study staff that
the consent was signed, then study staff will schedule initial baseline study visit.
Visit 1 and Visit 2 will take place at the RIOA at week 0 and week 24, respectively.
Participants will report having fasted overnight, and having abstained from alcohol for 24
hours, vigorous exercise for 24 hours, and caffeine for 12 hours. A blood sample will be
drawn upon arrival, followed by a DXA scan to measured bone mineral density (BMD) in both
hips and lumbar spine, and for body composition, using CTRAL equipment. Participants will
also undergo a body water assessment using BIA to determine deuterium dose. Bilateral
handgrip strength will be measured via Dynamometer. Participants will fill out a 3-Day food
log, physical activity questionnaire, pain scale, KOOS, VR-12, and the POMS. Participants
will be given an 8-week supply of their respective treatment supplement, with instructions
and a compliance log (to be filled out monthly). Participants will also be given their dose
of deuterium oxide (D2O) to be ingested according to instruction at week 2&3, prior to TKA
(week 4).
Tissue samples for ACL, bone fragments, and synovial fluid will be collected by the PI during
TKA surgery. All other assessments will be taken during clinical visits with the
participant's physical therapists and their orthopedic doctors. The PI will attend some of
these visits to assess wound healing, administer handgrip strength assessment, and to
replenish participant treatment supply.
UAMS Orthopedic Clinic personnel will monitor the clinic logs for prospective participants
meeting the inclusion/exclusion criteria of the study, notifying the study Principal
Investigator (PI) of potential study participants. The PI will meet with the with interested
participant to obtain consent virtually (via REDCap) prior to scheduling baseline visit (week
0) at the UAMS Reynolds Institute on Aging (RIOA). The potential study participant will be
allowed as much time as needed to be comfortable in their decision to participate in the
study.
For tissue specimen collection during TKA, the PI will attend the surgery, collecting samples
of the ACL, synovial fluid and bone fragments as they are removed (and would otherwise be
discarded) by the surgeon. Blood will also be collected by the anesthesiologist after line
placement in the operating room. Tissue samples will be prepared as described in the Specimen
Handling and Storage Section and taken to the PI's laboratory, the Center for Translational
Research in Aging and Longevity (CTRAL) located on the 7th floor of the UAMS RIOA (a secured
access floor).
Study Visits Week 0 (Baseline)
- Informed Consent (executed electronically)
- Randomization (Excel Randomization Function)
- Baseline assessments (CTRAL) Knee Injury and Osteoarthritis Outcome Score (KOOS)
Veterans RAND 12 (VR-12) Profile of Mood States (POMS) Physical Activity Pain Dietary
Intake (3-Day Food Log) Dual-energy X-ray absorptiometry (DXA) scan - bone density (both
hips and lumbar spine) Dual-energy X-ray absorptiometry (DXA) scan - body composition
Bioelectrical impedance analysis (BIA) Scan - body water Hand grip strength Collecting
blood sample (4 mL x 1 for serum and 4 mL x 1 for plasma)
- Treatment 10 g Collagen Peptides or Placebo, Weeks 0 - 24 Deuterated water (D2O), Weeks
6 - 8 Week 4
- Virtual
- Knee Injury and Osteoarthritis Outcome Score (KOOS)
- Veterans RAND 12 (VR-12)
- Profile of Mood States (POMS)
- Physical Activity
- Pain 3-day food log Compliance Week 8
- Virtual
- Knee Injury and Osteoarthritis Outcome Score (KOOS)
- Veterans RAND 12 (VR-12)
- Profile of Mood States (POMS)
- Physical Activity
- Pain 3-day food log Compliance
- Total Knee Arthroplasty Collect Anterior Cruciate Ligament Collect Synovial Fluid
Collect blood sample (4 mL x 1 for serum and 4 mL x 1 for plasma)
- Physical Therapy (three times weekly, Weeks 8 - 24) Pain Range of Motion (ROM) for
flexion and extension of surgery knee KOOS Jr. Week 10
- Physician Visit Wound healing Pain ROM for flexion and extension of surgery knee Grip
Strength Week 12
- Virtual
- Knee Injury and Osteoarthritis Outcome Score (KOOS)
- Veterans RAND 12 (VR-12)
- Profile of Mood States (POMS)
- Physical Activity
- Pain 3-day food log Compliance Week 14
- Physician Visit Wound healing Pain ROM for flexion and extension of surgery knee Grip
Strength Week 16
- Virtual
- Knee Injury and Osteoarthritis Outcome Score (KOOS)
- Veterans RAND 12 (VR-12)
- Profile of Mood States (POMS)
- Physical Activity
- Pain 3-day food log Compliance
- Physical Therapy Follow Up Pain ROM KOOS Jr. Functional Measures Battery Week 20
- Virtual
- Knee Injury and Osteoarthritis Outcome Score (KOOS)
- Veterans RAND 12 (VR-12)
- Profile of Mood States (POMS)
- Physical Activity
- Pain 3-day food log Compliance
- Physician Visit Wound healing Pain ROM for flexion and extension of surgery knee Grip
Strength Week 24 (Final Assessments - Stop Treatment)
- CTRAL Knee Injury and Osteoarthritis Outcome Score (KOOS) Veterans RAND 12 (VR-12)
Profile of Mood States (POMS) Pain Activity DXA - bone mineral density (both hips and
lumbar spine) DXA - body composition Grip Strength Compliance 3-Day Food Log
