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Table 4 Data collection timepoints and respective outcomes

From: A single-center, open-label, randomized, parallel-group trial to pilot the effectiveness of a peer coach behavioral intervention versus an active control in reducing anxiety and depression in patients scheduled for total knee replacement

 

Baseline

1-week pre- surgery

6-weeks post- surgery

6-months post-surgery

1-year post- surgery

2-years post-surgery

Sociodemographic information (collected via EHR and patient survey)

x

     

Medical history (collected via EHR and patient survey)

x

     

Surgical history (collected via EHR and patient survey)

x

     

Primary Outcomes – Patient-reported

 PHQ-8 (depression)

x

x

x

x

x

x

 GAD-7 (anxiety)

x

x

x

x

x

x

Secondary Outcomes – Patient-reported and/or electronic health record

 Resources used to prepare for surgery

x

x

    

 KOOS pain and ADL subscales

x

x

x

x

x

x

 Lubben Social Network Scale

x

x

x

x

x

x

 Short Form-12

x

x

x

x

x

x

 Pain Catastrophizing Scale

x

x

x

x

x

x

 General Self-Efficacy Scale

x

x

x

x

x

x

 Opioid use

x

x

x

x

x

x

 COVID-19 screener survey

x

x

x

x

  

 Exercise survey

x

x

x

x

x

x

 Sleep disturbance (PROMIS)

x

x

x

x

x

x

 Surgical outcomes

  

x

x

x

x

 Program Evaluation

  

x

x

x

x

 Knee range of motion

x

x

x

x

  

 Blood Pressure

x

x

x

x

  

 Resting Heart Rate

x

x

x

x

  

 Weight

x

x

x

x

  

 Timed up and go test

x

x

x

x

  

 6-min walk test

x

x

x

x

  

 30 second chair stand test

x

x

x

x

  

 Quadriceps Strength using a handheld dynamometer

x

x

x

x

  
  1. EHR Electronic health record, PHQ – 8 Patient Health Questionnaire 8 items, GAD-7 Generalized Anxiety Disorder 7 items, KOOS ADL Knee Injury and Osteoarthritis Outcome Score Activity of Daily Living Sub-scale, COVID-19 Coronavirus disease 2019, PROMIS Patient-Reported Outcomes Measurement Information System