Early Cognitive Changes After Same-day Discharge Hip and Knee Arthroplasty
NCT07598552
Cognition Disorders, Cognitive Change
Svendborg, Denmark
View Trial DetailsNCT Number: NCT07067060
SUMMARY
Background:
After knee arthroplasty (KA), rehabilitation is widely recommended, yet its clinical effectiveness-especially the need for supervision-has been challenged. While some argue that supervised rehabilitation may prevent serious adverse events (SAEs), previous trials show no superiority of rehabilitation, supervised or not, over no rehabilitation in terms of function. However, these trials were underpowered for safety outcomes. A large-scale evaluation is needed to determine if supervision impacts SAE risk, thereby informing rational use of health care resources.
Rationale for the proposed study. A conventional randomized trial to assess the safety of supervised versus unsupervised rehabilitation after KA would require an ethically and logistically infeasible sample size. By emulating such a trial using routinely collected registry data, the investigators can estimate the causal effect of supervision on the risk of serious adverse events-while accounting for confounding and preserving real-world relevance.
Actionable objective and hypothesis: To test whether unsupervised rehabilitation after knee arthroplasty increases the risk of serious adverse events over a 2-year period compared with supervised rehabilitation. The investigators hypothesize that unsupervised rehabilitation is non-inferior, defined as a hazard ratio for SAE risk below 1.4.
Design: Target trial emulation (TTE) using nationwide registry data to replicate the design and intent of a pragmatic randomized trial.
Setting: Danish hospitals and municipalities. Patients: Adults undergoing primary total or unicompartmental knee arthroplasty for osteoarthritis, identified from Danish registries. The target trial assumes consecutive recruitment at hospital discharge to mirror real-world referral practices.
Interventions: Referral to unsupervised home-based exercise or supervised municipal physiotherapy, defined by referral to rehabilitation pathways initiated at hospital discharge.
Methods: Primary outcome is serious adverse events; secondary is number of hospital contacts. Propensity score-based weighting will adjust for confounding using patient and administrative covariates (e.g. age, BMI, comorbidities, surgery year), enabling causal inference from observational data.
Results: Findings will inform clinical practice by estimating the comparative safety of unsupervised versus supervised rehabilitation after knee arthroplasty, based on real-world data from over 40,000 patients.
Limitations: As with all non-randomized studies, residual confounding is possible. Despite adjustment strategies, causal interpretations should be made with caution due to reliance on observational data.
Conclusion: While TTE can provide valuable insight, the causal inferences made with TTE should be interpreted with caution, when not supported with an RCT.
Funding: Section for Biostatistics and Evidence-Based Research, the Parker Institute, Bispebjerg and Frederiksberg Hospital is supported by a core grant from the Oak Foundation (OFIL-24-074).
External funding: in process. Registration: TBD (registration on ClinicalTrials.Gov)
Trial opening soon.
Get NotifiedAll sexes
Observational
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: 2 years
The term "serious adverse events" (SAE) is defined by the ICH framework as any untoward medical occurrence that, at any dose, results in: 1) death, 2) life-threatening conditions, 3) inpatient hospitalization or prolonged existing hospitalization, 4) persistent or significant disability/incapacity, or 5) congenital anomalies/birth defects.
Time frame: 2 years
The term "serious adverse events" (SAE) is defined by the ICH framework as any untoward medical occurrence that, at any dose, results in: 1) death, 2) life-threatening conditions, 3) inpatient hospitalization or prolonged existing hospitalization, 4) persistent or significant disability/incapacity, or 5) congenital anomalies/birth defects
Time frame: 2 years
Number of hospital contact
Copenhagen University Hospital, Hvidovre
Other
Risk of Serious Adverse Events Following Unsupervised vs Supervised Rehabilitation After Knee Arthroplasty: Protocol For An Emulated Noninferiority Trial (SAFE-T)
Acronym: SAFE-T
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT07598552
Cognition Disorders, Cognitive Change
Svendborg, Denmark
View Trial DetailsNCT05735847
Arthritis, Joint Diseases
Hvidovre, Denmark
View Trial DetailsNCT06124170
Agnosia, Arthritis
Chengdu, Sichuan, China
View Trial DetailsNCT06894719
Neurologic Manifestations, Pain
View Trial Details