DOI: https://doi.org/10.21203/rs.3.rs-172101/v1
Purpose
We conducted a randomised controlled trial (PhysSURG-B) to assess the short- and long-term effects of a non-supervised physical activity intervention at the time of breast cancer surgery. Here we report a secondary outcome, quality of life (QoL).
Methods
Female patients planned for surgery were randomly assigned to either an intervention of 30 minutes of self-administered physical aerobic activity daily 2 weeks before and 4 weeks after surgery, or control. QoL was assessed with questionnaires at baseline, 4 weeks and 12 months postop using the instruments FACT-B, RAND-36 and EQ-VAS.
Results
Out of 354 included participants at 12 months follow-up after surgery, 287 were available for QoL analysis. Comparing intervention to control, the results for the FACT- B score at 4 weeks showed an odds ratio (OR) of 0.975 (95% CI 0.636-1.495) and at 12 months an OR of 0.883 (95% CI 0.581-1.342). The subgroup of patients receiving adjuvant chemotherapy had significantly lower FACT-B at 12 months compared to no chemotherapy (OR 0.475, 95% CI 0.300-0.735). EQ-VAS showed OR 1.163 (95% CI 0.760-1.779) and 0.817 (95% CI 0.536-1.244) at 4 weeks and 12 months, respectively. RAND-36 domains “role limitations due to physical health” and “pain” showed a decrease at 4 weeks in both groups, returning towards baseline at 12 months follow-up.
Conclusion
An intervention of non-supervised physical activity before and after surgery for breast cancer had no effect on QoL. Patients receiving adjuvant chemotherapy had significantly lower QoL, regardless of study group.
Trial registration
ClinicalTrials.gov registration number: NCT 02560662. Registered 25 September, 2015.
Breast cancer affects more than 1.6 million women worldwide every year [1]. Following treatment, common side-effects are known to have negative impact on survivorship [2]. For proper management of patients, evaluating the effect of breast cancer treatment on survivorship is crucial [2]. Patient-reported outcomes (PROs) [3–5], such as quality of life (QoL), are especially important to assess [4, 5].
In observational studies, regular physical activity after breast cancer diagnosis has been associated with increased breast cancer-specific and overall survival [6–8]. In patients undergoing adjuvant treatment for breast cancer, interventions with physical exercise during or after treatment have been reported to reduce fatigue [9–11] and to increase QoL [12–15]. To our knowledge, there are no reports of large randomized trials of prehabilitation consisting of physical activity before breast cancer surgery which address short- and long-term QoL.
The aim of this study was to evaluate the effects on a secondary outcome, quality of life, of a self-administered intervention with pre- and postoperative physical activity compared with a control group, within 12 months after primary breast cancer surgery.
We report 4 weeks and 12 months follow-up data from the PhysSURG-B randomised, controlled, prospective interventional trial evaluating an intervention of added aerobic physical activity before and after breast cancer surgery. The study protocol and primary outcome of self-reported physical recovery at 4 weeks after surgery have been published elsewhere [16]. Participants were recruited from three surgical departments in the Western Region of Sweden between Nov 2016 and Dec 2018. Participants were randomised to intervention with non-supervised physical activity, or control.
Female patients ≥ 18 years, diagnosed with stage I-III breast cancer, scheduled for primary surgery were randomised into two groups, intervention and control. Exclusion criteria were male sex, stage IV disease, neoadjuvant treatment and inability to understand the study information or perform the intervention. Neither research nurses or participants were blinded, due to the nature of the intervention, but patient allocation was not actively briefed to healthcare personnel involved in the routine care of the patient.
The intervention in the PhysSURG-B trial has been described previously in detail [16]. In summary, patients in the intervention group received an individual consultation with a physiotherapist and were instructed to add 30 minutes of daily aerobic physical activity, 2 weeks ±1 week before and 4 weeks after breast cancer surgery. The intervention was instructed to be of medium intensity resulting in shortness of breath but with ability to talk, of the participant’s own choice after suggestions from the physiotherapist, and to be performed without supervision. In addition, two follow-up telephone calls were made during the intervention period. Added physical activity was registered in a diary. Adherence to the intervention was considered if registered physical activity was > 10 days preoperatively and > 20 postoperatively.
Participants in the control group were not advised regarding physical activity, but received standard information regarding early mobilization and shoulder movement after surgery according to standard care.
The level of physical activity was measured with the Saltin Grimby Physical Activity Level Scale (SGPALS) [17].
Patient-reported outcome measures of quality of life was a secondary outcome in the PhysSURG-B-trial, reported at three time points from which change from baseline to 4 weeks and 12 months respectively after surgery was calculated. The following validated instruments were used (Swedish versions):
Functional Assessment of Cancer Therapy-Breast Cancer (FACT-B) [18], including FACT-B Total Score, FACT General (FACT-G) Total Score and FACT-B Trial Outcome Index (TOI).
RAND 36-Item Health Survey 1.0 [19]
EuroQol- visual analogue scale (EQ-VAS) [20]
A single-item QoL question validated and used previously [21–23] asking “How would you describe your quality of life the last month?” Answering alternatives on a scale from ”0” (worst possible quality of life) to “6” (best possible quality of life).
The sample size calculation for PhysSurg-B was performed for the primary outcome measure of physical recovery 4 weeks after surgery. No sample size calculation was performed for the secondary outcome quality of life.
A statistical analysis plan was written before any of the analyses were performed. The analyses were according to randomisation (intention-to-treat analysis). Baseline demographic data (patient and tumour characteristics and type of surgery) were described per allocated group. Total scores and subscale scores of the QoL instruments were calculated. The scores (total score for FACT-B, EQ-VAS) had skewed and multi-modal distribution making a gaussian linear model invalid. Therefore, the effect of the intervention was estimated using an ordinal regression model [24]. The baseline measurements were included as a covariate along with fixed factors for study group, time and their interaction. The single item QoL question was dichotomised into “low QoL” (scale option 1–4) and “high QoL” (scale option 5–6) before analysis. For all instruments, the primary analysis was the unadjusted. Adjuvant chemotherapy was imbalanced across the study groups and therefore, as an additional analysis adjuvant chemotherapy was adjusted for. Also, a subgroup analysis of patients given adjuvant chemotherapy was conducted.
The results are presented as odds ratios (OR) for intervention scoring higher than the control with 95% confidence intervals (CIs). All tests were two-sided and a statistical significance level of 5% was used. We made no adjustments for multiple comparisons. No imputations were made. All statistical analyses were performed with SAS→ 9.4.
The Regional ethical review board in Gothenburg, Sweden approved the trial (registration numbers 522 − 15, T1152-16, T700-17, T160-18). The procedures used in this study adhere to the tenets of the 1964 Helsinki declaration with amendments. Informed consent was obtained from all individual participants included in the study. PhysSURG-B was registered at ClinicalTrials.gov (NCT 02560662) September 25, 2015.
The participant flow throughout the trial is visualised in Fig. 1. At 12 months after surgery 354/400 participants (88.5%) remained in the trial, 44 patients withdrew informed consent (18 in the control group and 26 in the intervention group) and one participant in each group had died. 297/354 (84%) returned their questionnaires (return rate 83–90% for the different timepoints), with no difference between the study groups. Complete data for QoL assessment at all three time-points was reported by 81% (287/354 participants), 148 in the control group and 139 in the intervention group respectively.
Baseline patient demographics, tumour characteristics and type of surgery were similar in the two study groups (Table 1 and Table 2). Median age was 63 years (mean 62 years, range 30–89 years). More than thirty percent of the participants reported a risk consumption of alcohol according to Alcohol Use Disorders Identification Test (AUDIT-C), and two thirds of the patients had at least one comorbidity where cardio-vascular disease was the most frequent. The majority of patients underwent breast-conserving surgery (79%) and sentinel lymph node biopsy (95%) (Table 2). To 94% of the participants, adjuvant treatment was given. Endocrine therapy was received by 76% in the control and 79% the intervention group, respectively. Radiotherapy was administered to 75% in the control and 83% in the intervention group, respectively. Adjuvant chemotherapy was given to 26 % in the control compared to 37% in the intervention group. No severe adverse events related to the intervention were reported. Adherence to the intervention registered as added physical activity (> 10 days and > 20 days before and after surgery) was less than 60% according to the physical activity diary. Physical activity level measured with SGPALS, at baseline and at the end of the intervention period, showed that 64% in the intervention and 66% in the control group did not report any changes in their physical activity level.
| CONTROL n = 148 | INTERVENTION n = 139 | |
|---|---|---|
| Age, years median (IQR) range | 64 (54–72) 38–89 | 62 (51–68) 30–84 |
| BMI, kg/m2 median (IQR) range missing | 25.0 19.0-38.5 8 | 24.6 17.7–47.6 11 |
| ASA I II III IV Missing | 58/148 (39%) 82/148 (55%) 8/148 (5%) 0 0 | 73/137 (53%) 62/137 (45%) 2/137 (1%) 0 2 |
| Comorbidities None Diabetes Cardiovascular disease Pulmonary disease Psychiatric illness Chronic pain | 52/142 (37%) 10/147 (7%) 48/142 (34%) 5/142 (4%) 25/142 (18%) 13/142 (9%) | 46/135 (34%) 8/139 (6%) 33/135 (24%) 10/135 (7%) 21/135 (16%) 11/135 (8%) |
| Active smoking Yes No Missing | 10/145 (7%) 135/145 (93%) 3 | 3/138 (2%) 135/138 (98%) 1 |
| Alcohol consumption AUDIT-C score < 4 AUDIT-C score ≥ 41 Missing | 94/143 (66%) 49/143 (34%) 5 | 93/137 (68%) 44/137 (32%) 2 |
| Physical activity at baseline2 1 (inactive) 2 (low) 3–4 (moderate-vigorous) Missing | 23/147 (16%) 97/147 (66%) 27/147 (18%) 1 | 18/137 (13%) 85/137 (62%) 34/137 (25%) 2 |
| Residence Rural Urban Missing | 13/147 (9%) 134/147 (91%) 1 | 13/138 (9%) 125/138 (91%) 1 |
| Educational level University education or higher 12 years or less Missing | 72/147 (49%) 75/147 (51%) 1 | 89/138 (64%) 49/138 (36%) 1 |
| ASA: American Society of Anesthesiologists, BMI: Body Mass Index, SGPALS: Saltin Grimby Physical Activity Level Scale | ||
| Valid percent given. | ||
| 1 Risk consumption level defined as AUDIT-C-score ≥ 4 | ||
| 2 Measured using SGPALS at baseline | ||
| CONTROL n = 148 | INTERVENTION n = 139 | |
|---|---|---|
| Type of breast surgery Breast conserving surgery Mastectomy Missing | 114/148 (77%) 34/148 (23%) 0 | 113/139 (81%) 26/139 (19%) 0 |
| Type of axillary surgery non-ALND1 ALND Missing | 142/148 (96%) 6/148 (4%) 0 | 131/139 (94%) 8/139 (6%) 0 |
| Tumour type Invasive cancer Cancer in-situ Other Missing | 137/148 (93%) 11/148 (7%) 0 0 | 129/139 (93%) 10/139 (7%) 0 0 |
| Tumour size (mm), median (IQR) | 16 (11–23) | 17 (11–25) |
| Estrogen receptor positive (ER+) | 118/148 (86%) | 114/139 (89%) |
| Progesterone receptor positive (PR+) | 103/148 (75%) | 97/139 (76%) |
| Her2-positive (HER2+) | 16/148 (12%) | 10/139 (8%) |
| Nodal metastasis (N+) | 26/148 (19%) | 36/139 (27%) |
| Adjuvant treatment, any Radiotherapy Chemotherapy Endocrine therapy Bisphosphonates Anti-Her-2-therapy Missing | 140/148 (95%) 111/148 (75%) 39/148 (26%) 113/148 (76%) 17/148 (12%) 12/148 (8%) 0 | 129/137 (93%) 113/137 (83%) 50/137 (37%) 108/137 (79%) 24/137 (18%) 10/137 (7%) 2 |
| ALND: Axillary Lymph Node Dissection, SGPALS: Saltin Grimby Physical Activity Level Scale | ||
| 1 Non-ALND includes Sentinel Lymph Node Biopsy and no axillary surgery | ||
FACT-B
At baseline, 4 weeks and 12 months the median FACT-B scores were 116.8, 121.5 and 121.9 in the control group, compared to 117.5, 121.0, 119.1 in the control group (Table 4). Comparing the intervention to the control group, the FACT- B score at 4 weeks showed an odds ratio (OR) 0.975 (95% CI 0.636–1.495) and at 12 months OR 0.883 (95% CI 0.581–1.342) (Table 3). When adjusted for adjuvant chemotherapy, the odds ratio at 12 months was 0.997 (95% CI 0.654–1.520). For the subset of patients who received adjuvant chemotherapy, a significantly lower FACT-B score at 4 weeks and 12 months was seen, with OR 0.418 (95% CI 0.260–0.670) and OR 0.475 (95% CI 0.300-0.753), respectively when compared to those who did not receive chemotherapy (Fig. 2), but with no significant difference based on study group. The FACT-G scores and the breast cancer subscales showed no difference over time or between the study groups (Table 4). FACT-G mean baseline scores were 86.2 for control and 85.7 for intervention (median 87.8 and 87.6, respectively).
| CONTROL n = 148 | INTERVENTION n = 139 | ||||||||
| Mean | Median | ±SD | Missing | Mean | Median | ±SD | Missing | ||
| FACT-B (0–148) | Baseline | 115.3 | 116.8 | 16.6 | 11 | 114.7 | 117.5 | 16.7 | 8 |
| 4 weeks | 117.0 | 121.5 | 18.2 | 8 | 116.3 | 121.0 | 20.0 | 10 | |
| Change1 to 4 weeks | + 1.8 | + 3.0 | 13.1 | + 2.5 | + 2.0 | 12.5 | |||
| 12 months | 116.3 | 121.9 | 20.3 | 2 | 115.8 | 119.1 | 19.9 | 3 | |
| Change1 to 12 months | + 1.3 | + 3.5 | 16.2 | + 0.9 | + 2.8 | 14.6 | |||
| FACT-G (0–108) | Baseline | 86.2 | 87.8 | 13.7 | 7 | 85.7 | 87.6 | 13.8 | 5 |
| 4 weeks | 88.5 | 93.0 | 14.6 | 8 | 87.2 | 92.0 | 16.4 | 10 | |
| 12 months | 88.4 | 93.0 | 16.3 | 0 | 87.8 | 92.0 | 15.6 | 2 | |
| Breast cancer Subscale (0–40) | Baseline | 28.8 | 29.0 | 4.5 | 5 | 28.9 | 30.0 | 4.5 | 5 |
| 4 weeks | 28.5 | 29.0 | 5.0 | 5 | 29.2 | 30.0 | 4.8 | 8 | |
| 12 months | 27.9 | 29.0 | 5.5 | 0 | 28.1 | 29.0 | 5.4 | 1 | |
| Physical well-being (0–28) | Baseline | 24.8 | 26.0 | 3.7 | 3 | 24.7 | 25.8 | 3.3 | 1 |
| 4 weeks | 24.1 | 25.0 | 3.8 | 6 | 24.0 | 26.0 | 4.5 | 8 | |
| 12 months | 23.8 | 25.0 | 4.6 | 0 | 23.4 | 24.8 | 4.6 | 1 | |
| Emotional well-being (0–24) | Baseline | 16.5 | 17.0 | 4.9 | 2 | 16.8 | 18.0 | 4.8 | 1 |
| 4 weeks | 19.3 | 20.0 | 4.6 | 6 | 18.7 | 20.0 | 5.2 | 9 | |
| 12 months | 20.0 | 21.0 | 4.0 | 1 | 20.1 | 21.0 | 3.9 | 2 | |
| Social well-being (0–28) | Baseline | 24.2 | 25.7 | 3.8 | 5 | 23.7 | 25.0 | 4.4 | 1 |
| 4 weeks | 24.7 | 25.8 | 3.9 | 6 | 23.9 | 25.0 | 4.3 | 9 | |
| 12 months | 23.2 | 24.3 | 5.1 | 2 | 22.8 | 24.0 | 4.6 | 1 | |
| Functional well-being (0–28) | Baseline | 20.5 | 21.0 | 5.1 | 2 | 20.4 | 21.0 | 5.5 | 0 |
| 4 weeks | 20.4 | 21.0 | 5.7 | 6 | 20.8 | 22.0 | 5.6 | 8 | |
| 12 months | 21.4 | 22.0 | 5.6 | 0 | 21.6 | 22.5 | 5.3 | 1 | |
| FACT-B TOI | Baseline | 74.2 | 76.5 | 10.9 | 8 | 73.9 | 76.0 | 11.3 | 6 |
| 4 weeks | 73.0 | 75.0 | 12.7 | 7 | 73.9 | 78.0 | 13.4 | 8 | |
| 12 months | 73.1 | 77.0 | 13.6 | 0 | 73.0 | 77.0 | 13.8 | 2 | |
| FACT-B: Functional assessment of cancer therapy-breast, FACT-G: Functional assessment of cancer therapy- General, TOI: Trial Outcome Index, SD: Standard deviation | |||||||||
| 1Change from baseline | |||||||||
| Odds Ratio Intervention/Control (95% CI) | |||
|---|---|---|---|
| Baseline | 4 weeks | 12 months | |
| FACT-B Crude Adjusted1 | 1.023 (0.676–1.550) | 0.975 (0.636–1.495) 1.073 (0.697–1.651) | 0.883 (0.581–1.342) 0.997 (0.654–1.520) |
| EQ-VAS Crude Adjusted1 | 0.869 (0.576–1.312) | 1.163 (0.760–1.779) 1.254 (0.816–1.926) | 0.817 (0.536–1.244) 0.852 (0.559-1.300) |
| QoL question2 Crude | 0.91 (0.25–3.32) | 1.07 (0.30–3.86) | |
| FACT-B: Functional assessment of cancer therapy-breast, total score. CI: Confidence Interval | |||
| 1adjusted for adjuvant chemotherapy 2 Dichotomised into “low QoL” and “high QoL” | |||
EQ-VAS
EQ-VAS median score was 80 at all timepoints, and there were no differences seen between the study groups (Table 5). During the active part of the intervention (from baseline to 4 weeks postop), the odds ratio was 1.163 (95% CI 0.760–1.779) for the intervention compared to the control group. At 12 months the OR was 0.817 (95% CI 0.536–1.244), and adjusted for chemotherapy 0.852 (95% CI 0.559-1.300) (Table 3). For all participants regardless of study group, EQ-VAS at 4 weeks had an OR of 0.557 (95% CI 0.350–0.886), and at 12 months an OR 0.656 (95% CI 0.417–1.032) for chemotherapy compared to no chemotherapy.
| CONTROL N = 148 | INTERVENTION N = 139 | |||||
|---|---|---|---|---|---|---|
| Mean (Min - Max) | Median | ± SD | Mean (Min - Max) | Median | ± SD | |
| Baseline | 76 (5–100) | 80 | 18.0 | 73 (0–100) | 80 | 20.0 |
| 4 weeks | 76 (20–100) | 80 | 18.0 | 75 (20–100) | 80 | 19.0 |
| Change1 to 4 weeks | − 0.0 (-50–40) | ± 0 | 15.8 | + 3.2 (-60–90) | ± 0 | 18.2 |
| 12 months | 79 (30–100) | 80 | 17.0 | 76 (27–100) | 80 | 19.0 |
| Change1 to 12 months | + 2.5 (-55–45) | ± 0 | 16.0 | + 2.8 (-40–98) | ± 0 | 20.2 |
| SD: Standard deviation | ||||||
| 1 from baseline | ||||||
RAND-36
RAND-36 declined in the domains “role limitations due to physical health” and “pain” at 4 weeks postoperatively, with no difference between the study groups. At 12 months participants had to a large extent resumed their QoL (Fig. 3 and Supplementary Table 1).
Analysis of the dichotomised QoL question, “How would you describe your quality of life the last month?” resulted in no difference between the intervention and control group, neither at 4 weeks (OR 0.91, 95% CI 0.25–3.32) nor at 12 months (OR 1.07, 95% CI 0.30–3.86) (Table 3).
The results from this randomized trial examining the effect of moderate physical activity as prehabilitation in women undergoing breast cancer surgery did not show effects on QoL at 4 weeks or 12 months after surgery. Previous studies on QoL during adjuvant treatment [15] have primarily investigated effects following supervised, high intensity exercise interventions for a longer period of time [11]. Even with such intense exercise interventions, significant improvements in quality of life have not been reported [11]. This may in part be explained by a high baseline level of QoL in breast cancer patients, as also seen in our trial, and difficulties to detect and/or discriminate improvements from this level. The aim of our trial was to investigate the effect of a simple non-supervised intervention, in keeping with national and international recommendations regarding physical activity [25]. The intervention was chosen, assumed to be easily implementable and with slight impact on the care pathway for breast cancer treatment.
The FACT-G score in our trial cohort revealed a higher level of QoL, with a mean baseline score of 86, compared to 77 in the normative data for the general Swedish female population sample (pro-rated mean FACT-GP scores) [26]. The FACT-G minimally important difference (MID) is considered to be approximately 5–6 in a breast cancer population, with a MID 7–8 for the total FACT-B score [27]. The higher FACT-G score in our sample of breast cancer patients could suggest a selection bias, where individuals with lower QoL declined participation. Another possible explanation is the difference in age distribution in our study sample (mean 62 years) compared to the population sample (mean 49 years), as a higher age was positively correlated to higher FACT-GP score. Moreover, the FACT-G and FACT-B scores we present are similar to previously published results for breast cancer patients [28–30]. Over time, the FACT-B scores were stable regardless of study group and treatment factors, except for the subgroup of patient receiving adjuvant chemotherapy, where a significant decline was seen. Interestingly, this was not only seen at 12 months but also at 4 weeks, when the participants had not yet started their adjuvant chemotherapy but had gained information about the projected start of treatment.
EQ-VAS median score was stable regardless of study group and time for assessment and all changes seen in mean scores were less than the MID of 8 for EQ-VAS [31]. RAND-36 showed a temporary decline in the domains “Pain” and “Role limitations due to physical health” at 4 weeks, these changes were not seen at 12 months where participants had resumed their QoL. Interestingly, the domain “Emotional well-being” showed even better results at 12 months compared to baseline, possibly as a result of improved adaptive strategies and response shift over time. The domain “General health” improved during the active intervention period at 4 weeks after surgery, but at 12 months returned to baseline.
The consistency in FACT-B and EQ-VAS score from baseline to 4 weeks after surgery could indicate an inability of the instruments to encompass or discriminate changes resulting from the surgical insult, or that breast cancer diagnosis and surgery alone in fact has low impact on QoL. A significant difference was only seen for patients receiving adjuvant chemotherapy, compared to patients not receiving adjuvant chemotherapy, suggesting that this is a subgroup of patients that may benefit more from interventions aimed at improving QoL.
The strengths of the current study include the randomized controlled design, the use of several validated QoL instruments, both generic and disease specific, as well as both short- and long-term follow-up. Limitations include the lack of objective measures of physical activity, regarding type, duration and/or intensity of physical activity. Low adherence to the intervention, confine the effects of this non-supervised intervention and point to the draw-backs of recommendations regarding exercise, in line with previous studies [11, 32]. Our results, in accordance with previous findings seem to suggest the need for improved strategies and additional support in order to achieve the recommended physical activity level for patients with breast cancer.
Based on the results from these and previously presented outcomes of this trial we cannot advocate for prehabilitation including a recommendation of physical activity into guidelines for patients awaiting surgery for breast cancer.
ASA American Society of Anesthesiologists
AUDIT-C Alcohol Use Disorders Identification Test
BMI Body Mass Index
CI Confidence Interval
EQ-VAS EuroQol- visual analogue scale
FACT-B Functional Assessment of Cancer Therapy-Breast Cancer
FACT-G Functional Assessment of Cancer Therapy-General
FACT-GP Functional Assessment of Cancer Therapy-General Population
MID Minimally Important Difference
OR Odds ratio
PRO Patient-reported outcome
QoL Quality of life
RAND-36 RAND 36-Item Health Survey 1.0
SGPALS Saltin Grimby Physical Activity Level Scale
SD Standard deviation
TOI Trial Outcome Index
Funding This study was funded by Sahlgrenska University Hospital (ALFGBG-4307771, ALFGBG-718221), AFA Insurance (150072), The Swedish Cancer Society (CAN 2016/362, 2020/ 19 0303), The Gothenburg Medical Society (GLS 779001, GLS 879101), Lions Cancer Research Fund of Western Sweden (LCV2018:28), Anna-Lisa and Bror Björnssons Foundation and Knut and Alice Wallenberg Foundation.
Conflict of Interest The authors declare that they have no conflicts of interest.
Availability of data and material The datasets generated during and/or analysed during the current study are available from the corresponding author on reasonable request.
Code availability Not applicable
Authors’ contributions All authors contributed to the study conception and design. Material preparation, data collection and analysis were performed by Jenny Heiman, Eva Haglind and Roger Olofsson Bagge. The first draft of the manuscript was written by Jenny Heiman and all authors commented on previous versions of the manuscript. All authors read and approved the final manuscript.
Ethical approval All procedures performed involving human participants were in accordance with the ethical standards of the institutional and national research committee (Regional Ethical Review Board in Gothenburg, Sweden, registration numbers: 522-15, T1152-16, T700-17, T160-18) and with the 1964 Helsinki declaration with amendments.
Consent to participate Informed consent was obtained from all individual participants included in the trial.
Consent for publication Not applicable
Acknowledgements
We extend our gratitude to the participants in the PhysSURG-B trial, the physiotherapists involved in the intervention, as well as research nurses and all personnel involved in conducting the trial at the including hospitals.