Veterans Enhanced Recovery Using Integrative Treatments Around Surgery

Trial statusNot yet recruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age18+
SponsorDurham VA Medical Center

About this trial

The study aims to assess the implementation and effectiveness of Integrative Treatments - Music Medicine, Aromatherapy, and Battlefield Acupuncture - in the management of perioperative pain and anxiety, and in the reduction of related pharmacologic treatments.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Veterans Scheduled to undergo procedures at the Durham VA

Disqualifiers

Hearing Loss

Procedures on the Ear

Risk of Bleeding

Anosmia

Trial design

Design model

Parallel

Treatments tested in this trial

  • Nonpharmacologic Treatment

    Other intervention

    At least one three nonpharmacologic treatments (Music Medicine, Aromatherapy, Battlefield Acupuncture) will be delivered. Music Medicine is the delivery of personal music players to listen to patient-preferred music before, during, or after surgical or non-surgical procedures. Aromatherapy is the delivery of personally-preferred AromaTabs before, during, or after surgical or non-surgical procedures. Battlefield Acupuncture is the delivery of Auricular Acutherapy by trained providers using acupuncture needles or acupressure beads before, during, or after surgical or non-surgical procedures.

  • Standard Care

    Other intervention

    Patients will receive standard clinical care without the addition of Music Medicine, Aromatherapy, or Battlefield Acupuncture

Treatment groups

400 Participants
are divided into 2 treatment groups
Group A: Integrative TreatmentActive comparator 1 intervention
Group B: Standard CareActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Pain and Pain Interference assessed among patients using the Defense veterans pain rating scale 2.0

The Defense and Veterans Pain Rating Scale 2.0 utilizes a numerical rating scale enhanced by functional word descriptors, color coding, and pictorial facial expressions matched to pain levels. Four supplemental questions measure how much pain: a) interferes with usual activity, b) interferes with sleep, c) affects mood and d) contributes to stress. The scale for each assessment ranges from 0-10. Three assessments will occur each day. The daily average values will be compared at each time point. Higher Scores represent worse outcomes.

Time frame
Each day from Postoperative Day 0 to Day 5.
2

Heart Rate Variability among Patients as assessed using time and frequency domain analysis of the heart rate.

Heart rate variability represents the change in the time interval in milliseconds between successive heartbeats. It is a measure of input to the heart from both sympathetic and parasympathetic branches of the nervous system. Increased heart rate variability is the better outcome.

Time frame
Each day (over 8-hour periods, 7pm and 7am) from 5 days before surgery to postoperative day 5.
3

Implementation of Treatment among Patients as assessed by the Acceptability of Intervention, Appropriateness of Intervention, and Feasibility of Intervention Measures.

The Acceptability of Intervention measure, Appropriateness of Intervention measure, and Feasibility of Intervention Measure will be used. Each of these three tools is a 4-item questionnaire that has been validated as a distinct and strong measure of implementation success. Scale values for each measure range from 1-5. The average of the three measures will be computed and compared at each time point. Higher scores represent better outcomes.

Time frame
Measurement will be at three points: within the 5 day period before surgery; on the day of Surgery; and on postoperative day 5.
4

Fidelity of Treatment among Patients as assessed by a Fidelity Checklist

Fidelity, the degree to which an intervention was implemented as it was intended by the developers, will be measured using a fidelity instrument with three domains: adherence (adherence to each component of treatment, scale 1- 5), participant responsiveness (measured on the treatment expectation questionnaire scale 0-10), and dosage (scale 1-5). Higher scores are better. We will compare the average scores overall, and in each domain.

Time frame
Each day from Postoperative Day 0 to Day 5.

Secondary outcomes

1

Amount of Opioid medication received by patients assessed in average daily oral morphine equivalents.

The amount of opioid analgesic medications received by patients as recorded in the electronic health record (inpatient setting) or as reported by patients (outpatient setting) will be summarized each day and reported in daily oral morphine equivalents. The total amount from postoperative day 0 to day 5, and the average daily oral morphine equivalents will be measured for comparisons. Higher amounts represent worse outcomes.

Time frame
Each day from Postoperative Day 0 to Day 5.
2

Quality of Recovery among patients as measured using the Quality-of-Recovery 40 tool.

The Quality-of-Recovery 40 tool is a 40-item questionnaire, with each question graded on a five-point Likert scale. Scores range from 40 (extremely poor quality of recovery) to 200 (excellent quality of recovery). Assessment will occur preoperatively on the day of surgery (baseline value) and each day from Postoperative Day 0 to 5. The difference between the baseline and the value each day will be compared.

Time frame
Preoperative on the day of surgery, and each day from Postoperative Day 0 to Day 5.

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

This trial is not recruiting at the moment. You can still explore other options: