Setting and Study Design
A retrospective evaluation of a tertiary cancer centre cohort, analysing prospective data collected between March 2019 (allied health service commencement) to March 2020.The model of standard care is detailed in Figure 1.
Program development:
Staff delivering the service were physiotherapists/exercise physiologists (EPs), dietitians and clinical psychologists with an average of 3, 5 and 4 years specialist oncology experience respectively. Further information about program development and staff training is in supplementary file 2.
Procedure
Intervention component reporting follows the Template for Intervention Description and Replication (TIDiER) [14] guidelines as described in supplementary file 3.
Patients, referral and enrolment:
Eligible patients were adults being considered for high dose chemotherapy and AuSCT in the haematology service who were medically and cognitively able to participate in exercise.
The allied health service was initiated as part of routine care by the clinical haematology AuSCT team; the planned referral pathway involved the AuSCT nurse consultant referring all eligible patients following acceptance into the AuSCT service by haematologists. Patients were telephone screened by a clinician, for exercise program eligibility using the validated Australian-modified Karnofsky Performance Status (AKPS) [15]. Scores range between 10 and 100 (higher reflecting improved function), based on the patients’ ability to perform regular tasks relating to activity, work, and self-care. Patients with an AKPS <50 were ineligible. Patients with bone involvement were eligible if cleared to exercise by their haematologist. Psychology eligibility screening was completed using the patient health questionnaire (PHQ-4), a valid tool for detecting anxiety and depressive disorders [16]. Patients were eligible for clinical psychology if they scored > 2 (mild distress).
Eligible patients were then invited to participate in the service and those accepting were booked for individual assessments with each discipline and clinical psychologist if eligible. Program duration was individualised, depending on the timing of referral in relation to medical treatment interventions.
Exercise Intervention:
An initial, individual assessment (60-minute) at the hospital was conducted. Supplementary file 4 presents safety criteria for starting and ceasing supervised exercise assessments/exercise. Treatment was commenced at initial assessment after baseline measures were completed. An individually tailored exercise program consisting of continuous moderate intensity aerobic and resistance exercise was prescribed. The exercise intervention was based upon initial assessment findings and aimed to progress towards meeting the Exercise and Sports Science Australia [17] recommendations of 150 minutes of moderate-intensity aerobic exercise and two resistance exercise sessions per week. Supplementary file 5 provides further details. Patients completed the program either independently at home, in a local gym, supervised at a community health centre or at the hospital gym. The program location was determined by patient residential location and preference and level of supervision needed. Programs were progressed to maintain moderate intensity, with weekly/fortnightly telehealth or phone reviews. Program adherence was monitored using patient self-report.
Nutrition intervention:
Initial assessment considered relevant clinical, anthropometric and biochemical markers, dietary intake, and estimation of nutritional requirements. The nutrition intervention consisted of 20-minute individualised sessions (hospital or phone), with the goals of care including maintenance/improvement in nutrition status. Intervention included medical nutrition therapy, information about the benefits of nutrition prehabilitation, prescription of relevant therapeutic diet, educational materials (supplementary file 6) and nutrition prehabilitation goal setting. Between 1-4 follow up appointments were scheduled if indicated at initial assessment, and treatment modifications were based on outcome changes.
Clinical Psychology intervention:
A full psychological initial assessment (60-minute, hospital) with individualised psychological support based on findings. Between 1-7 hospital follow-up appointments were scheduled and interventions included cognitive behavioural approaches to managing worry and pain, maintaining motivation, and activating supports in preparation for AuSCT.
Outcomes:
Evaluation of the impact of the prehabilitation program was measured using the RE-AIM framework (reach, effectiveness, adoption, implementation and maintenance). Table 1 describes the evaluation method for each dimension of the framework. Effectiveness outcomes are described below.
Effectiveness Outcomes as part of the RE-AIM framework measurements:
Patients completed outcome measures at baseline (T0, referral), pre-transplant (T1) and 30 days post-procedure (T2). The 6MWT is a commonly used submaximal test of functional exercise capacity [18] and is valid and reliable in cancer patients [19]. The 6MWT was completed using a 30-meter corridor and standardised encouragement. The Baseline Lite Hydraulic handgrip dynamometer (Fabrication Enterprises Inc.) was used to assess hand-grip strength and data from this device correlates with the Jamar dynamometer [20], which has demonstrated validity and reliability in the oncology population [21]. The validated 30-second sit-to-stand test (30secSTS), performed according to standard protocols, assessed lower limb strength and function [22].
Nutritional status was measured using the valid and reliable Patient-Generated Subjective Global Assessment (PG-SGA) [23] and percentage weight change. HRQoL was measured using the European Organisation for the Research and Treatment of Cancer Quality of Life Questionnaire Core 30 (EORTC-QLQ-C30)[24]. The International Physical Activity Questionnaire-Short Form (IPAQ-SF) is a reliable and valid [25] self-reported tool that assesses physical activity (PA) level.
Data management and analysis:
A research electronic data capture (REDCap) database was used [26]. Descriptive statistics were reported as counts and percentages, means and standard deviations or medians and interquartile ranges, as appropriate, to summarise variables. The change in objective and patient-reported measures from initial assessment (baseline) to pre-procedure was assessed using paired t-tests or the Wilcoxon signed rank test depending on the data distribution normality (continuous) and Mc Nemar’s test (categorical). No analyses involved all three time points. All tests of significance (p<0.05) performed are described and no adjustment was made for the number of outcomes assessed [27].