RCT on T-REX Twente Regimen Effects on Quality of Life and Mobilisation for Cardiac Surgery Patients After Sternotomy

Sponsor
Medisch Spectrum Twente (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT06115759
Collaborator
Foothills Medical Centre (Other)
200
1
2
27
7.4

Study Details

Study Description

Brief Summary

The goal of this study is whether the T-REX Twente precautions have a positive impact on the quality of life (MAcNew QLMI), level of physical activity, and reduction of fear of movement in heart patients after a total median sternotomy compared to the (current) standard precautions? Do these precautions also have no adverse effects on pain, wound healing, and/or postoperative complications?

Participants will be instructed by the physiotherapist to both groups immediately postoperatively and are constantly repeated by the involved disciplines during the hospital stay.

The control group is not allowed to lift, push, or pull for the first 6 weeks. There is little to no evidence for the current strict precautions currently implemented in the department.

The intervention group receives the new T-REX Twente precautions, allowing for more independent activities through the use of the tube model (keeping elbows close to the sides).

All patients receive three questionnaires (MacNew QLMI, Numeric Pain Rating Scale, and Tampa Scale for Kinesiophobia) preoperatively, on the 4th day postoperatively, on the first day of cardiac rehabilitation, and at the end of cardiac rehabilitation, taking approximately 10 minutes each time. Additionally, during the clinical admission immediately postoperatively, two AX3 accelerometers are placed on the patient, one lateroproximal on the right upper arm and one anterodistal on the right upper leg.

Researchers will compare heart patients after a total median sternotomy with T-REX Twente precautions (intervention group) to the (current) standard precautions (control group).

Condition or Disease Intervention/Treatment Phase
  • Behavioral: T-REX Twente precautions
  • Behavioral: Usual (restrictive) sternal precautions
N/A

Detailed Description

Each year, more than 1000 open-heart surgeries (OHO) are performed at Thorax Centrum Twente (TCT), with 860 of them involving a total median sternotomy. Some patients present themselves at the cardiac care unit with unexplained complaints after discharge, possibly caused by anxiety and insecurity.

There is no consensus regarding postoperative sternal precautions following a total median sternotomy. Studies in the United States and Canada have indicated that these precautions might be too strict, and alternative, less restrictive precautions through the use of the "Keep your Move in the Tube" (KYMITT) approach have been shown safe and without adverse consequences.

Although no statistically significant differences were observed in all outcomes, patients following the new approach (KYMITT) reported fewer issues with functional mobility.

This is a prospective randomized double blind study, collecting data from patients undergoing a total median sternotomy from November 2023 to November 2025 at TCT and concurrently participating in outpatient cardiac rehabilitation under the guidance of TCT.

Previous research using the MacNew quality of life questionnaire among 677 cardiac rehabilitation patients indicated that the difference in response was normally distributed with a standard deviation of 0.25. The KvL-H is the Dutch (validated) translation of the MacNew QLMI. Assuming an effect size of 0.25 (small to medium effect size) across the 4 measurement moments (T0, T2, T4, T5) between the two groups (grouptime interaction), a total of 178 patients were needed, i.e. 89 per group. This was based on a Repeated measures ANOVA with an alpha of 0.05, a power of 0.85 and a nonsphericity correction of 1, calculated with GPower 3.1.9.7. To account for a 10% dropout, 100 patients per group will be included.

A previous study on intensified walking during cardiac rehabilitation after acute myocardial infarction showed a KvL-H increase of 0.9 at the time of discharge (our study: T3) to intake cardiac rehabilitation (our study: T4) from 5.2 to 6.1 at the time of T5. A KvL-H increase of 0.46 points is expected in our T-REX Twente sternal precautions group (intervention group).

For the second primary endpoint, the relative percentage of daytime (between 6:00 and 23:00) non-bedtime up to and including 4 days postoperatively on the ICU and nursing ward is examined. From previous research in a similar population, it was observed that a relative rate of lying in bed of 60% is measured on day 1 after discharge from ICU, with a decrease of 6.5% per day (p < 0.001). Assuming a medium f2 effect size of 0.15 with a linear mixed model, two-sided testing, alpha of 0.05, power of 0.80 and two predictors (time and group), 68 patients are needed. To account for 10% dropout, 75 patients per group will be included.

The highest number of patients will be retained, i.e. 100 patients per group.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
200 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Outcomes Assessor)
Masking Description:
Patients will not be actively informed on their study arm, but will receive conventional or interventional rehabilitation instructions, and might be able to deduct their allocation arm. The researcher will be blinded for intervention or control group allocation.
Primary Purpose:
Treatment
Official Title:
A Randomized Clinical Trial to Study the "T-REX Twente Regimen" (Thoracic Surgery Rehabilitation Experts Twente) on Quality of Life and Mobilisation Activities for Cardiac Surgery Patients After Median Sternotomy, Compared to Usual Care
Anticipated Study Start Date :
Nov 1, 2023
Anticipated Primary Completion Date :
Jan 1, 2026
Anticipated Study Completion Date :
Feb 1, 2026

Arms and Interventions

Arm Intervention/Treatment
Experimental: T-REX Twente

The intervention group receives the new T-REX Twente precautions, allowing for more independent activities through the use of the tube model (keeping elbows close to the sides).

Behavioral: T-REX Twente precautions
The intervention group receives the new T-REX Twente precautions, allowing for more independent activities through the use of the tube model (keeping elbows close to the sides).
Other Names:
  • The T-REX Twente precautions are inspired on the Keep Your Move in the Tube (KYMITT) principle, and adjusted and improved to our local setting
  • Active Comparator: Usual care

    The control group is not allowed to lift, push, or pull for the first 6 weeks. There is little to no evidence for the current strict precautions currently implemented in the department.

    Behavioral: Usual (restrictive) sternal precautions
    The control group is not allowed to lift, push, or pull for the first 6 weeks. There is little to no evidence for the current strict precautions currently implemented in the department.

    Outcome Measures

    Primary Outcome Measures

    1. Quality of Life after Myocardial Infarction Questionnaire (MacNew QLMI) [Postoperative day 4 to start of cardiac rehabilitation (4-6 weeks postoperatively)]

      The first primary endpoint is the standardized response mean difference of Quality of Life after Myocardial Infarction Questionnaire (MacNew QLMI) clinically postoperative (4th day postoperatively) until the start of cardiac rehabilitation (4-6 weeks postoperatively). MacNew QLMI scores on a 7-pointscale (1-7), where 1 = always and 7 = never. MacNew QLMI is an ordinal scale, with a total sumscore of 189 points as the maximum quality of life.

    2. Not lying in bed [Postoperative day 4 to start of cardiac rehabilitation (4-6 weeks postoperatively)]

      The second primary endpoint is the duration of not being in bed for up to 4 days in the ICU and the general ward, measured using two AX3 accelerometers.

    Secondary Outcome Measures

    1. Numeric (Pain) Rating Scale (NPRS) [Preoperative to end of cardiac rehabilitation (12 weeks postoperatively)]

      Difference in experienced pain (self-reported) as measured with NPRS It is an 11-point ordinal scale (0-10) with 0 = no pain whatsoever, 10 = the worst pain most pain imaginable.

    2. Quality of Life after Myocardial Infarction Questionnaire (MacNew QLMI) [Preoperative to end of cardiac rehabilitation (12 weeks postoperatively)]

      Difference in QoL as measured with MacNew QLMI. MacNew QLMI scores on a 7-pointscale (1-7), where 1 = always and 7 = never. MacNew QLMI is an ordinal scale, with a total sumscore of 189 points as the maximum quality of life.

    3. Tampa Scale for Kinesiophobia (TSK) [Preoperative to end of cardiac rehabilitation (12 weeks postoperatively)]

      Difference in kinesiophobia as measured with TSK. The questionnaire consists of 17 items where a higher score represents a higher degree of fear of movement.

    4. Individual mobilisation activities as measured with AX3 Accelerometer [Postoperative (directly after surgery, day 0) until hospital discharge (expected to be around postoperative day 5 to a maximum of 7 days)]

      During clinical admission immediately postoperatively, two AX3 accelerometers are placed on the patient, one lateroproximal on the right upper arm and one anterodistal on the right upper leg. Mobilisation activities include: lying in bed, sitting on a chair, standing, walking, cycling on a bike ergometer, walking the stairs.

    5. Composite endpoint of sternal refixation, superficial and deep sternal wounds for 30 days after surgery [30-days postoperative]

      Definitions according to Netherlands Heart Registration

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Adult patients who are preoperatively included if they are undergoing a total median sternotomy at Thorax Centrum Twente (TCT)

    • Patients with their treating cardiologist also working for TCT.

    Exclusion Criteria:
    • 72 hours of admission to the Intensive Care Unit (ICU)

    • Postoperative delirium (diagnosed with Diagnostic and Statistical Manual of Mental Disorders (DSM) version V

    • Patients with dementia (or other significant cognitive disorders)

    • Dutch language barriers

    • Patients with a cardiologist from a location other than TCT

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Thoraxcentrum Twente Enschede Overijssel Netherlands 7500KA

    Sponsors and Collaborators

    • Medisch Spectrum Twente
    • Foothills Medical Centre

    Investigators

    • Principal Investigator: Frank R. Halfwerk, MD, PhD, Medisch Spectrum Twente, Enschede, the Netherlands

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Frank Halfwerk, Assistant Professor and Technical Medical Doctor in Cardio-Thoracic Surgery, Medisch Spectrum Twente
    ClinicalTrials.gov Identifier:
    NCT06115759
    Other Study ID Numbers:
    • T-REX Twente
    • CCMO-ABR 78107
    First Posted:
    Nov 3, 2023
    Last Update Posted:
    Nov 7, 2023
    Last Verified:
    Nov 1, 2023
    Individual Participant Data (IPD) Sharing Statement:
    Yes
    Plan to Share IPD:
    Yes
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Frank Halfwerk, Assistant Professor and Technical Medical Doctor in Cardio-Thoracic Surgery, Medisch Spectrum Twente
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Nov 7, 2023