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The Scientific World Journal logoLink to The Scientific World Journal
. 2014 Oct 28;2014:451935. doi: 10.1155/2014/451935

Effects of a Multidisciplinary Educational Rehabilitative Intervention in Breast Cancer Survivors: The Role of Body Image on Quality of Life Outcomes

Giovanni Morone 1, Marco Iosa 1, Augusto Fusco 1, Antonella Scappaticci 2, Maria Rosaria Alcuri 2, Vincenzo Maria Saraceni 2,3, Stefano Paolucci 1, Teresa Paolucci 2,3,*
PMCID: PMC4227364  PMID: 25405222

Abstract

In breast cancer survivors, own body image may change due to physical and psychological reasons, worsening women's living. The aim of the study was to investigate whether body image may affect the functional and quality of life outcomes after a multidisciplinary and educational rehabilitative intervention in sixty women with primary nonmetastatic breast cancer who have undergone conservative surgery. To assess the quality of life was administered The European Organization for Research and Treatment of Cancer Study Group on Quality of Life core questionnaire, while to investigate the psychological features and self-image were administered the following scales: the Body Image Scale, the Hamilton Rating Scale for Depression, and the State-Trait Anxiety Inventory. To assess the recovery of the function of the shoulder were administered: the Disabilities of the Arm, Shoulder, and Hand Questionnaire and the Constant-Murley Score. Data were collected at the baseline, at the end of the intervention, and at 3-month follow-up. We found a general improvement in the outcomes related to quality of life, and physical and psychological features after treatment (P < 0.001). During follow-up period, a higher further improvement in women without alterations in body image in respect of those with an altered self-perception of their own body was found (P = 0.01). In conclusion, the body image may influence the efficacy of a rehabilitative intervention, especially in the short term of follow-up.

1. Introduction

Breast cancer (BC) is the most common cancer among women, affecting more than 1.2 million individuals per year worldwide [1]. In recent years, there was a progressive decrement in mortality due to the continuous improvements in early detection of disease and its clinical care [2]. The consequent increasing survival rate implies the growing need for rehabilitative treatments of the short- and long-term sequelae, especially in the upper limb [3]. In the literature, a wide variation in the prevalence of these sequelae has been reported for shoulder pain (from 12 to 51%), for reduction of the range of shoulder motion (from 2 to 51%), and for muscle strength (from 17 to 33%) [4]. All these features may influence the patients' quality of life (QoL) [4], which has been found worsened one year after diagnosis of BC, and that could be influenced in turn by psychological factors, such as body image and mood disturbance [5].

In recent years, a number of growing studies have been focused on body image issues in cancer, such as among BC patients [6]. Body image is an emerging topic in the scientific literature that describes a cognitive dynamic perception of physical appearance of own body [7]. In patients having undergone BC surgery, body image was found altered not only after surgical treatments (mastectomy or partial mastectomy), but also after radiation and/or chemotherapy especially for redness and/or soreness and hair loss and/or weight gain [8]. By now, it should be weighed by surgeons and clinicians in the option of treatment [9, 10]. Low body image, attractiveness, and femininity positively have been found correlated with depression, impacting negatively QoL among women with breast cancer [11].

At the same time, rehabilitation has become an integrative part of the clinical care of people after BC surgery, both for the treatments of motor and for health-related QoL aspects [12]. In fact, exercise interventions are fundamental to improve the motor and psychological sequelae during treatment and in the post treatment rehabilitation period, as recently highlighted by recent Cochrane reviews on this topic [1214]. A multidisciplinary educational treatment was found to be effective in improving functional abilities and wellbeing and also during the follow-up period after BC surgery [15]. An educational intervention is defined as implying a brief contact with healthcare professionals, self-management patient-led groups, provision of educational booklets, and also Internet discussion groups [16]. It has been shown as psychoeducational group intervention, and physical activity can diminish fatigue and improve energy level, emotional distress at 3-month follow-up, and, finally, the overall QoL following intervention [17].

The direct effect of body image on the effectiveness of a rehabilitative intervention has received far too little attention. It is conceivable that an altered body image may deteriorate the quality of life and functional outcomes of a rehabilitative treatment [18]. Women after BC may experience body shame and being more vulnerable to psychological distress and may experience poorer adjustment after BC treatment [19].

The aim of this study was to investigate the influence of body image on the quality of life related outcomes after a multidisciplinary and educational rehabilitative intervention and at 3-month follow-up in group after breast cancer surgery. At the same time, the secondary aim of our study was to investigate whether the psychological features (as body image, depression, and anxiety) may influence the response to the rehabilitation treatment with objectives like the reduction of pain and the improvement of shoulder function of the operated side.

2. Materials and Methods

In the present study we have hypothesized that the alteration of the body image perception could have a negative impact on quality of life and on rehabilitative effectiveness in women affected by the sequelae of breast cancer.

2.1. Participants

We have screened consecutive patients referred to physiatrist outpatient consultant for rehabilitation after breast cancer intervention. Inclusion criteria were women with diagnosis of primary nonmetastatic breast cancer having undergone conservative surgery (complete local excision and axillary dissection) or modified radical mastectomy, with age ranging between 18 and 75 years old, with mild to moderate lymphoedema and/or functional limitation of the ipsilateral shoulder. Women were involved in the study at least six months after surgery, and during this period they did not perform any rehabilitative treatment.

Exclusion criteria were active, locoregional recurrence and/or bilateral breast cancer, women without axillary lymph node dissection, concurrent chemotherapy or radiotherapy, preexisting neuromuscular or musculoskeletal conditions affecting local upper extremity testing and/or performance, presence of mastitis and/or lymphangitis, systemic disease, and no previous treatment or contraindication to physiotherapy.

Each patient was assessed at baseline (T 0), at the end of treatment (T end), and at a three-month follow-up (T f-up) by the same physician. Efficacy of rehabilitative intervention has been analysed on the entire sample, as detailed below. Then, following the aim of our study, participants were also divided into two groups during data analysis, those with an altered self-perception of body image (Body Image Scale BIS > 10; see below for details) and those without alterations in self-perception of body image (BIS ≤ 10). Among psychological features, anxiety and depression were investigated and analysed.

This trial was approved by the local ethical committee and it was submitted to National Ministry of Health as clinical trial of our institution. An informed consent was signed by patients before participation in the study.

2.2. Rehabilitation

Rehabilitation consisted of a multidisciplinary intervention of ten sessions of physiotherapy which lasted around 45 minutes, carried out 2 times a week, into 40 days. Exercise interventions could be defined as moderate to vigorous, in accordance with what was reported by Mishra and colleagues [12]. Sessions were performed by trained physiotherapists on subgroups of patients including 4 or 5 participants each.

Interaction among patients and personal care was encouraged to recreate self-help groups for greater sharing of the experience of illness, and self-management programs could help to increase patients' self-efficacy for better self-management. Physiotherapists tailored rehabilitation regarding patients' functional problems (i.e., lymphedema, reduction of the shoulder range of motion, and pain) and guided the motor rehabilitation. The exercises' protocol is analytically outlined in Table 1. The educational intervention was adapted to enhance the patients' knowledge of the sequelae of BC and to improve the self-care skills to be autonomous in the management of sequelae of BC.

Table 1.

Exercises' program.

Exercise Description
Exercise 1
Relaxing
Diaphragmatic breathing and postural elements such as alignment of the midline.
The patient is supine on a mat with flexed knees and arms along the chest.

Exercise 2
Raising arm, opening and closing punches
Lying on the bed, arms at sides, flexed knees. Slowly, lift parallel the arms till the upright position, opening and clenching the fists in order to contract the muscles of the arms. Maintain up the position, opening and closing the punches five times, and return to the starting position. Repeat ten times.

Exercise 3
Stretching and releasing the arms. Recovery of the flexion.
Lying on the bed, flexed knees. Interlock the fingers and slowly bring to full flexion and then on the pillow; then put as much as possible while keeping your arms extended. Perform the technique of breathing for a minute. Repeat ten times.

Exercise 4
Turn the shoulders. Rotation-anteropulsion-retropulsion
Standing or sitting, rotate the shoulders for ten times.

Exercise 5
Abduction and adduction of the arms—isometric strengthening
Lying or standing, bring the arms out, with extended elbows. Maintain the position for six seconds. Return to the starting position, slowly. Repeat for ten times.

Exercise 6
Opening and closing elbows
Standing, legs apart. Place both hands on the hips with thumbs pointing backwards. Push your elbows back and forth without moving the hands. Repeat for ten times.

Exercise 7
Run up the wall—recovery of flexion
Getting closer to the maximum height possible completely to the wall, stopping for few seconds, and trying to gently remove the hands from the wall. Repeat ten times.

Exercise 8
Run up the wall by the side—recovery of abduction
With a bit of tape, standing with the unaffected side facing the wall, place the hand on the wall at shoulder height. Reaching a point with his hand, as high as possible, marking it with the piece of tape. Begin the exercise with the operated arm, and repeat ten times trying to get closer to the mark left on the wall.

Exercise 9
Hand on the operated shoulder—recovery of the adduction
Sitting or standing, arms along the sides. Bring the hand of the operated limb to the contralateral shoulder. Return to starting position. Repeat ten times.

Exercise 10
Rotate the arms—promoting the rotations
Standing with legs apart, raise your arms to the shoulder. Beginning with small movements, gradually increase the diameter up to do it without complaints. We recommend at least five full rotations. Finally, bring the arm down the side and remain at rest for a moment.

Exercise 11
Run up the back—promoting the extension and intrarotation
Standing, place the hands behind the back and take with the healthy hand, the hand of the operated limb. Slowly slide the hands along the spine upwards to its possible and maintain the position for a few seconds. Then decline slowly. Repeat for ten times.

Exercise 12
Opening and closing the elbows
Standing or sitting, with the feet firmly on the ground, interlock the hands ahead of face with the head upright. Slowly, raise the arms above the head and then behind the neck. Then open both elbows and close them for five times. If you feel discomfort at the wound, keep the position and work with the breathing.

Exercise 13
Bar
Sitting or standing, hold the bar (about 110 cm long). Bring the arms forward and upward at the elbows extended. Flex elbows and bring the bar behind the head. Return slowly to starting position. Repeat ten times.

Exercise 14
Codman's pendulum
Lying on a bed in a prone position, the arm perpendicular to the floor, make a circular motion clockwise and counterclockwise slowly. Repeat for ten times.

Exercise 15
Flex on the front wall—to prevent the deficit of the scapula
Standing in front of the wall, put the hands against the wall parallel. Flex the arms. Repeat for ten times.

Contents and details were merged with Green's Precede model of health behavior, already used in these patients [20, 21]. The protocol was developed to respond to the collective postoperative care and patients' needs and no personal psychological treatment was planned. Precede model was incorporated into our rehabilitative program by including the use of effective strategies to correct motor habit, promote restorative activities, reduce fatigue, improve patients' knowledge and skills to enable them to perform self-care, promote a balance between activity, exercise, and rest, and finally share with other members of the group beliefs, attitudes, and perceptions.

During the first session, general anatomical details as well as information about lymphedema, limitation of range of motion of the shoulder, and medical and psychological suggestions were provided. Influencing factors, as beliefs, attitudes, and perceptions, were outlined and the following themes were focused on: “what may happen after a breast cancer operation,” “how to prevent lymphedema,” “how to prevent menopausal side effects of hormonal therapy,” “normal crisis reactions,” and “body image and sexual issues.” At the end of the rehabilitation, patients were invited to continue the exercises at home, with the same frequency and in the same way.

2.3. Quality of Life Assessment

2.3.1. European Organization for Research and Treatment of Cancer Study Group on Quality of Life Core Questionnaire

The European Organisation for Research and Treatment of Cancer Quality of Life core questionnaire (EORTC QLQ-C30) [22] is the global cancer-specific questionnaire which is used to examine the health-related quality of life among patients with cancer. This is a 30-item core questionnaire, used to assess the physical and psychosocial functioning and symptom experiences. This scale has been validated and revised several times. The questionnaire is divided into five functional scales (physical, role, emotional, cognitive, and social functioning) and nine symptoms' scales and single items (fatigue, nausea/vomiting, pain, dyspnoea, insomnia, appetite loss, constipation, diarrhoea, and financial difficulties). The acquired scores of each scale are spread in the 0–100 domain. A higher score in the functional scales indicates a better function, and in the symptom scales, it indicates a more intensive symptom [23]. For the Italian population, the reliability and the validity were found adequate [24]. The EORTC QLQ-C30 was the primary outcome measure of this study.

2.4. Psychometric Assessment

2.4.1. Body Image Scale

The Body Image Scale (BIS) [9] is a 10-item reliable measure developed to assess affective, behavioural, and cognitive dimensions of body image in cancer patients. It uses a 4-point response scale and the final score is the sum of the 10 items, ranging from 0 to 30, with zero scores representing no symptom or distress and higher scores corresponding to increasing symptoms and distress or more body image concerns. We used the median value of the recorded scores to dichotomize them during the analysis of variance. BIS-score was used to dichotomize women in those with altered (BIS-score > 10) and those with unaltered body image (BIS ≤ 10). This division was performed to assess the effect of body image on the effectiveness of therapy in terms of EORTC QLQ-C30 improvement.

2.4.2. Hamilton Rating Scale for Depression

The Hamilton Rating Scale for Depression (HAM-D) [25] is the most popular depression assessment instrument, for both children and adults. It has been demonstrated to be a reliable and a valid standard for symptom burden presence. This scale includes core features of depression, such as low mood and loss of interest in usual activities, and associated features such as anxiety and hypochondriac concerns. At least twenty published versions of the scale exist, including both longer and shortened versions. We used the original version proposed by Hamilton with 17 items, which is the most consistent in detecting change and is validated in Italian [26]. Values higher than 7 were reported as indicating presence of depression [27]; for this reason we have dichotomized the Hamilton scale-scores in 0 if <7 and 1 otherwise for analysis of variance.

2.4.3. State-Trait Anxiety Inventory

The State-Trait Anxiety Inventory (STAI) consists of 20 items referring to self-reported state anxiety and 20 items to trait anxiety [28] and was validated in Italian [29]. It is a reliable and well-validated measure of acute anxiety. The evaluated qualities are feelings of apprehension, tension, nervousness, and worry. Higher scores indicate the presence of anxiety: if the score is more than 40, the trait of anxiety is pathologic [28]. We used this cut-off value to dichotomize the STAI-score during analyses of variance.

2.5. Functional Assessment

2.5.1. Disabilities of the Arm, Shoulder, and Hand Questionnaire

The Disabilities of Arm, Shoulder, and Hand Questionnaire (DASH) [30] is a 30-item, self-report questionnaire designed to measure physical functions and symptoms in people with any of several musculoskeletal disorders of the upper limb. It quantifies the general disabilities related to the upper extremity. The items are related to the degree of difficulty in performing various functional activities because of arm, shoulder, or hand troubles (21 items), the severity of pain, activity-related pain, tingling, weakness, and stiffness (5 items), and the effect on social activities, work, and sleep and its psychological impact (4 items). Each item has 5 response options, ranging from 1 to 5. The responses to the 30 items are summed to form a raw score that is then converted to a 0-to-100 scale. A higher score reflects greater disability. The use of Disabilities of Arm, Shoulder, and Hand Questionnaire has rapidly increased in clinical trials and the instrument is available in several languages, Italian included [31].

2.5.2. Constant-Murley Score

The Constant-Murley Score (CMS) is one of the most used, valid, and reliable outcome measures for the assessment of the shoulder [26]. This scoring system consists of subjective variables, such as pain (15 points), activities in daily living (10 points), and arm positioning (10 points) and objective variables, such as range of motion (40 points) and strength (25 points).

2.5.3. Statistical Analysis

An intention to treat analysis was performed on participants who performed at least 4 therapy sessions, as shown in Figure 1. Friedman analyses and Wilcoxon tests for post hoc analyses were performed to assess the variations of scale-scores during time. Mann-Whitney U test was performed to test scale-scores between different groups of participants (chemotherapy versus no chemotherapy and mastectomy versus quadrantectomy). Spearman coefficient was computed to assess the correlation between scale-scores. Pearson coefficient (R) was computed to assess correlation with the effectiveness, a continuous variable.

Figure 1.

Figure 1

Study flowchart.

An analysis of variance was performed on the European Organisation for Research and Treatment of Cancer QLQ-C30 effectiveness using as factors the three dichotomized psychological scale-scores (Hamilton Rating Scale for Depression >7, State-Trait Anxiety Inventory >40, and Body Image Scale >10). Effectiveness reflects the proportion of potential improvement that was achieved during rehabilitation, calculated as [(discharge score − initial score)/(maximum score − initial score)] × 100. Thus, if a patient achieved the highest possible score after rehabilitation, the effectiveness was 100%.

3. Results

3.1. Sample Characteristics

During a period of 24 months, eighty-one patients were assessed. Seventy-two patients were enrolled into the study and assigned to the intervention. During treatment, twelve patients were dropped out. None complained about pain. Because these 52 patients did not participate just in a number of sessions between one to a maximum of three, none of them was considered a drop-out, and, applying an intention to treat approach, all the sample of 60 included patients was analysed (see Figure 1). Sample size was not pre-defined, but determined by the period of observation of the study, that is, 2 years.

The mean age of participants was 59.48 ± 11.10 years old. The mean time from previous surgery was 2.1 ± 1.7 years: 45% of the sample have undergone a mastectomy, and 55% have undergone a quadrantectomy. In 72% of the cases, patients have undergone a complete axillary dissection, while the sentinel lymph node has been removed in 27% of them and some lymph node intervention occurred in 1% of the patients. All patients performed a previous period of radiotherapy, while only 55% of the sample performed chemotherapy. Demographic and clinical characteristics are shown in Table 2, including the scales-scores recorded at T 0, at T end, and at T f-up.

Table 2.

Demographic and clinical characteristics of the sample. Cases (and percentages) or mean ± standard deviation of demographic and clinical characteristics of the sample. Median (1st; 3rd quartiles) for the scale scores. T 0: baseline; T end: end of treatment; T f-up: three-month follow-up; QoL: quality of life; DASH: Disabilities of the Arm, Shoulder, and Hand Questionnaire; BIS: Body Image Scale; HAM-D: Hamilton Rating Scale for Depression; CMS: Constant-Murley Score; EORTC QLQ-C30: Quality of Life core questionnaire (GH: global health; FS: function scale; SS: symptom scale); STAI: State-Trait Anxiety Inventory.

Demographic characteristics
 Number of patients 60
 Age [years] 59.48 ± 11.10
 Body mass index [kg/m2] 26.42 ± 3.85
 Married/common-law wife 46 (77%)
 Working, not employed, or retired 43 (72%)
 High school or master degree education 36 (60%)
Clinical characteristics
 Quadrantectomy 33 (55%)
 Mastectomy 27 (45%)
 Chemotherapy 33 (55%)
 Radiotherapy 60 (100%)
 Lymphatic drainage 10 (17%)
 Years from surgery [years] 2.11 ± 1.70
Scale-scores T 0 T end T f-up
EORTC QLQ-30 GH 66 (50; 75) 66 (57; 83) 75 (64; 83)
EORTC QLQ-30 FS 76 (58; 83) 83 (72; 87) 84 (71; 92)
EORTC QLQ-30 SS 20 (13, 28) 13 (7; 21) 11 (3; 18)
CMS 54 (39; 61) 67 (60; 72) 73 (66; 79)
DASH 40 (17; 59) 30 (10; 48) 18 (4; 40)
HAM-D 9 (4; 11) 7 (3; 11) 6 (1; 10)
STAI 44 (40; 48) 40 (38; 45) 40 (36; 44)
BIS 10 (4; 19) 8 (3; 17) 8 (2; 16)
Effectiveness T 0T end T endT f-up
EORTC QLQ-30 GH 16 (0; 32) 15 (0; 32)
EORTC QLQ-30 FS 15 (7; 35) 9 (0; 24)
EORTC QLQ-30 SS −7 (−11; −3) −2 (−6; 0)

3.2. Changes in Quality of Life and Functional and Psychological Scales

Quality of life of our patients significantly improved after rehabilitation (χ 2 = 52.29, P < 0.001), as shown in Figure 2. This improvement significantly occurred both between T 0 and T end (P = 0.001) and between T end and T f-up (P = 0.004). The functional scores recorded during the rehabilitative pathway were significantly improved in terms of both CMS (χ 2 = 103.38, P < 0.001, Friedman analysis) and DASH (χ 2 = 93.27, P < 0.001). Post hoc analysis revealed significant improvements observed between T 0 and T end for all the scales (P < 0.001), and during the follow-up period, a successive improvement was found significant for CMS (P < 0.001) and for DASH (P < 0.001) (see Figure 2).

Figure 2.

Figure 2

Box and whiskers plot of the scale-scores related to the physical and psychological features of the patients recorded at baseline (T 0), at end of treatment (T end), and after three months of follow-up (T f-up). Each box represents first and third quartile values together with the bold line representing the median values; whiskers represent the minimum and maximum values, and the circles are the values considerable by outliers (not excluded but analysed). CMS: Constant-Murley Score, DASH: Disabilities of the Arm, Shoulder, and Hand Questionnaire, EORTC QLQ 30: EORTC Quality of Life core questionnaire, HAM-D: Hamilton Rating Scale for Depression questionnaire, STAI: State-Trait Anxiety Inventory, and BIS: Body Image Scale.

The psychological scores were significantly reduced in terms of HAM-D (χ 2 = 64.50, P < 0.001), STAI (χ 2 = 25.06, P < 0.001), and BIS (χ 2 = 37.26, P < 0.001). In particular, for all the recorded scales, a significant improvement in psychological status was observed between T 0 and T end (P < 0.001 for all of them). During the follow-up period, a successive improvement was found significant for CMS (P < 0.001), DASH (P < 0.001), EORTC QLQ-C30 (P = 0.004), and HAM-D (P < 0.001), but neither for BIS- (P = 0.043, not statistically significant for Bonferroni correction) nor for STAI-scores (P = 0.062). As shown in Table 2 and Figure 2, median values of BIS-score did not change between T end and T f-up, despite quartile values and, hence, the data distributions around medians were quite different in the two assessments.

3.3. Factors Affecting Psychological Characteristics at Baseline

At T 0 many correlations were found between psychological scale-scores (BIS and HAM-D: ρ = 0.397, P = 0.002; BIS and STAI: ρ = 0.293, P = 0.022, HAM-D; and STAI: ρ = 0.565, P < 0.001). Only the BIS-score was significantly different between women who underwent a chemotherapy intervention (17; quartiles: 9; 22 versus 5; quartiles: 2; 9,  P < 0.001, Mann-Whitney U test) and between those who underwent a mastectomy (19; quartiles: 10; 22) versus quadrantectomy (6; quartiles: 3; 11, P < 0.001). The STAI-scores (P = 0.247, P = 0.087, resp.), such as HAM-D scores (P = 0.238, P = 0.402, resp.), were not affected by these factors. Then, the BIS-score was not affected by the presence of lymphedema (P = 0.382).

3.4. Effects of Psychological Characteristics on the Quality of Life Related Outcome

A significant correlation with time from surgery was found only for the effectiveness of treatment in terms of STAI (R = −0.346, P = 0.007): longer was the time from surgery and lower was the effect of treatment on anxiety reduction. An analysis of variance performed on the effectiveness of treatment in terms of EORTC QLQ-C30 general health using BIS-score as binary factor (BIS ≤ 10: not altered body image versus BIS > 10: altered body image) showed a significant effect on the increment during follow-up (i.e., between T end and T f-up) of the BIS-score achieved at the end of treatment T end  (F(1,58) = 5.841, P = 0.019), whereas during treatment period (i.e., between T 0 and T end), the baseline BIS-score (i.e., at T 0) was not significant (F(1,58) = 0.124, P = 0.726). As shown in Figure 3, the effectiveness of treatment was positive (improvement) between T 0 and T end (on the left) and between T end and T f-up (on the right). If during training all participants, independently from their BIS-score, improved their QoL of about 20% of the maximum possible improvement, in the three months after rehabilitation those with a normal perception of their body image (BIS ≤ 10) seemed to benefit more from the treatment with an ulterior improvement of 30% in their QoL, whereas those with an altered perception of body image had a slight improvement of 10%.

Figure 3.

Figure 3

Mean and standard deviation of the effectiveness of the treatment in terms of EORTC QLQ 30 Global Health: EORTC Quality of Life core questionnaire in the treatment period (on the left) and during the follow-up period (on the right) for the patients with Body Image Scale (BIS) scores ≤ 10 (black bars) and >10 (grey bars) at baseline.

4. Discussion

The primary aim of this study was to investigate if the alteration in the body image perception may affect the outcomes related to quality of life after a multidisciplinary educational rehabilitative intervention in women who have undergone breast cancer surgery. We found that, during rehabilitation, body image did not affect the rehabilitative outcomes related to quality of life. Conversely, it had a significant role at follow-up, with a higher further improvement in women without alterations in body image in respect of those with an altered self-perception of their own body (as shown in Figure 3). As expected, both functional and psychological features of the patients improved after rehabilitation. Also the BIS changed significantly during the rehabilitative period, but no further significant changes were recorded during follow-up period. In fact, the effectiveness of treatment was higher for patients with a less altered body image at the follow-up. Although neither body image nor changes in body image were found significantly correlated with time from surgery, this time was found significantly correlated with the benefits obtained in terms of anxiety reduction after treatment, suggesting the need of an early rehabilitative intervention. Body image was found the only factor significantly correlated with the effectiveness of the treatment in terms of quality of life. Neither depression nor anxiety was related to QoL-related outcomes, although before treatment all psychological aspects resulting were strictly related to each other. In particular, body image was found to be influenced by anxiety and depression at the beginning of this study.

Time from surgery was found inversely correlated to the benefits in terms of anxiety reduction after treatment, suggesting the need of an early rehabilitative intervention. Body image was the only factor influenced by the type of surgery (mastectomy or quadrantectomy) and chemotherapy intervention (present or not). Before rehabilitation, our results showed higher levels of alterations in body image, probably related to appearance dissatisfaction and reduced attractiveness, in women treated with mastectomy rather than with quadrantectomy and in those who underwent chemotherapy. In our data, the baseline body image was not influenced by the presence of lymphedema. This result agreed with Speck and colleagues [32] but not with a recent review on this topic [33]. This was probably due to the fact that our patients had a mild stage of lymphedema and were enrolled in mean more than one year after surgery. In add, Speck and colleagues [32] found an improvement in body image perception after rehabilitative intervention (twice a week for 13 weeks), but they did not find any improvement in QoL. Our results suggest that it was the level of body image perception that could affect the further improvement of QoL during the follow-up period. It should be noted that, at the end of the rehabilitation, our patients were invited to continue the exercises at home, with the same cadence and in the same way. But in this period, the lack of a rehabilitative supervision could have increased the affecting role of self-perception.

Our results support the idea that, before the intervention, the medical staff should carefully take into account the body image that each patient experiences. In fact, patients affected by breast cancer have a multidimensionality of the problems like functional, psychological, and social ones which make this disease one of the best candidates for multidisciplinary intervention. The multidimensionality of the problem implied that the intervention changed the body image that, in turn, could affect the effectiveness of the intervention in a complex dance of circular causation. Then, the multidisciplinarity implies the need of an educational part of the intervention as time spent in knowing patients' needs and in providing correct information for managing sequelae and side effects during rehabilitation as well as after rehabilitation with a pamphlet, similarly to previous interventions [3436]. As strongly affirmed in the cancer rehabilitation, the intervention should aim at achieving full functional, psychological, social, and educational improvement for the patients within the limits imposed by the disease [37]. These psychological features seem to play a fundamental role especially when patients finish their rehabilitative course and they feel more alone and vulnerable.

The findings of this study must be taken into account in light of the limitations. First of all, this study lacks a control group performing another type of intervention. In fact, even if rehabilitation in small groups has been demonstrated to be effective in the motor outcomes for other diseases, as low back pain and osteoporosis [34, 36, 38], it is conceivable that, performing exercises tailored for a single patient, both functional and psychological outcomes could be superior. Then, the interaction among patients and between patients and personal care, which is possible in the small groups, was encouraged but not documented. Hence, this fundamental aspect of the group rehabilitation cannot be precisely analyzed. Finally, the psychological aspects have been taken into account in relation to the body image. Nevertheless, these features may affect the functional outcomes in a wide spectrum of pathologies, from cancer to orthopaedic and neurological diseases [36, 39, 40]. Further studies should better analyze these aspects.

Our sample size of 60 patients is consistent with previous studies present in the literature. At the same time, it has to be noted as it was heterogeneous in terms of time from intervention. This is an aspect quite common for studies in the field of cancer rehabilitation, which could be impacting the results. Further investigations with a broader number of participants involved in these studies, with the use of an appropriate control group and stricter inclusion/exclusion criteria are warranted, especially in this type of patients, who may be evaluated as chronic. For the specific above-cited limits, we can consider our study as a feasibility trial, which highlights the relationship between different aspects of patient experiences. Due to our results, in the future, larger scale randomized controlled trials are needed. In view of the follow-up of just three months, our patients can be considered chronic and the results from the point of view of rehabilitation can be considered stable after these periods of observation. Finally, we did not analyze the effect of age. In fact, recently, it has been demonstrated that even there are significant improvements in physical functioning after a rehabilitative intervention, older women perceived relatively little improvement in QoL compared to younger women, and age had a differential negative influence on improvements in QoL [41]. However, this condition overstates our aim. In the next studies, also demographic and social features (as age, ethnicity, level of education, occupation, marital status, and occupation) should be taken into account as a factor influencing the functionality and QoL-related outcomes after the rehabilitation. Patients work on their body and with their body through specific exercise. Rehabilitation buy a new awareness of the injured part to improve body image.

Nevertheless, our study showed that rehabilitation, even when not performed immediately after the surgical treatment, is effective at the end of the intervention. At follow-up, further improvements were found only in subjects without alterations in body image. Further studies should also plan a psychological treatment during rehabilitative intervention targeted to improve body image, which has been shown by our results to be a prognostic factor for quality of life related outcomes.

5. Conclusions

Our results showed that the body image perception did not affect the efficacy of a rehabilitative intervention from baseline to the end of treatment, but it affected the potential further improvement occurring during the follow-up period, when women were probably more vulnerable. Then, we found that body image, depression, and anxiety resulting are significantly correlated to each other at baseline. Despite this, body image was the only factor affected by the type of surgical intervention and chemotherapy and it was the only factor affecting quality of life related outcomes.

In conclusion, considering the psychological aspects of the patients before planning a patient-tailored rehabilitative pathway may improve the efficacy of the rehabilitative intervention. In particular, own body image perception should be considered another treatment target for maintaining the improved level of quality of life of these patients.

Acknowledgments

The authors thank Carlo Tirelli (Department of Gynecology, San Carlo of Nancy Hospital, Rome, Italy) for his assistance as surgeon and for patient recruitment and ANTARES association. This study was supported by the Italian Ministry of Health (Grant 2011G), by Santa Lucia Foundation, and by “La Sapienza” University of Rome.

Conflict of Interests

The authors have declared the absence of any direct financial relation with ANTARES association and the absence of any other possible conflict of interests. All authors attest and affirm that the material within has not been and will not be submitted for publication elsewhere.

References

  • 1.Cheema B., Gaul C. A., Lane K., Fiatarone Singh M. A. Progressive resistance training in breast cancer: a systematic review of clinical trials. Breast Cancer Research and Treatment. 2008;109(1):9–26. doi: 10.1007/s10549-007-9638-0. [DOI] [PubMed] [Google Scholar]
  • 2.Gill D., Bruce D., Tan P. H. Controlling the cost of breast cancer. European Journal of Cancer Care. 2011;20(6):703–707. doi: 10.1111/j.1365-2354.2011.01289.x. [DOI] [PubMed] [Google Scholar]
  • 3.Eyigor S., Karapolat H., Yesil H., Uslu R., Durmaz B. Effects of pilates exercises on functional capacity, flexibility, fatigue, depression and quality of life in female breast cancer patients: a randomized controlled study. European Journal of Physical and Rehabilitation Medicine. 2010;46(4):481–487. [PubMed] [Google Scholar]
  • 4.Lee T. S., Kilbreath S. L., Refshauge K. M., Herbert R. D., Beith J. M. Prognosis of the upper limb following surgery and radiation for breast cancer. Breast Cancer Research and Treatment. 2008;110(1):19–37. doi: 10.1007/s10549-007-9710-9. [DOI] [PubMed] [Google Scholar]
  • 5.Shimozuma K., Ganz P. A., Petersen L., Hirji K. Quality of life in the first year after breast cancer surgery: rehabilitation needs and patterns of recovery. Breast Cancer Research and Treatment. 1999;56(1):45–57. doi: 10.1023/A:1006214830854. [DOI] [PubMed] [Google Scholar]
  • 6.Zimmermann T., Scott J. L., Heinrichs N. Individual and dyadic predictors of body image in women with breast cancer. Psycho-Oncology. 2010;19(10):1061–1068. doi: 10.1002/pon.1660. [DOI] [PubMed] [Google Scholar]
  • 7.Pruzinsky T. Enhancing quality of life in medical populations: a vision for body image assessment and rehabilitation as standards of care. Body Image. 2004;1(1):71–81. doi: 10.1016/S1740-1445(03)00010-X. [DOI] [PubMed] [Google Scholar]
  • 8.Winters Z. E., Benson J. R., Pusic A. L. A systematic review of the clinical evidence to guide treatment recommendations in breast reconstruction based on patient-reported outcome measures and health-related quality of life. Annals of Surgery. 2010;252(6):929–942. doi: 10.1097/SLA.0b013e3181e623db. [DOI] [PubMed] [Google Scholar]
  • 9.Hopwood P., Fletcher I., Lee A., Al Ghazal S. A body image scale for use with cancer patients. European Journal of Cancer. 2001;37(2):189–197. doi: 10.1016/S0959-8049(00)00353-1. [DOI] [PubMed] [Google Scholar]
  • 10.Annunziata M. A., Giovannini L., Muzzatti B. Assessing the body image: relevance, application and instruments for oncological settings. Supportive Care in Cancer. 2012;20(5):901–907. doi: 10.1007/s00520-011-1339-x. [DOI] [PubMed] [Google Scholar]
  • 11.Begovic-Juhant A., Chmielewski A., Iwuagwu S., Chapman L. A. Impact of body image on depression and quality of life among women with breast cancer. Journal of Psychosocial Oncology. 2012;30(4):446–460. doi: 10.1080/07347332.2012.684856. [DOI] [PubMed] [Google Scholar]
  • 12.Mishra S. I., Scherer R. W., Snyder C., Geigle P. M., Berlanstein D. R., Topaloglu O. Exercise interventions on health-related quality of life for people with cancer during active treatment. The Cochrane Database of Systematic Reviews. 2012;8 doi: 10.1002/14651858.CD008465.pub2.CD008465 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Payne C., Wiffen P. J., Martin S. Interventions for fatigue and weight loss in adults with advanced progressive illness. Cochrane Database of Systematic Reviews. 2012;1 doi: 10.1002/14651858.CD008427 [DOI] [PubMed] [Google Scholar]
  • 14.Mishra S. I., Scherer R. W., Geigle P. M., et al. Exercise interventions on health-related quality of life for cancer survivors. Cochrane Database of Systematic Reviews. 2012;8 doi: 10.1002/14651858.CD007566.pub2.CD007566 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Koinberg I., Langius-Eklöf A., Holmberg L., Fridlund B. The usefulness of a multidisciplinary educational programme after breast cancer surgery: a prospective and comparative study. European Journal of Oncology Nursing. 2006;10(4):273–282. doi: 10.1016/j.ejon.2005.11.005. [DOI] [PubMed] [Google Scholar]
  • 16.Brox J. I., Storheim K., Grotle M., Tveito T. H., Indahl A., Eriksen H. R. Systematic review of back schools, brief education, and fear-avoidance training for chronic low back pain. Spine Journal. 2008;8(6):948–958. doi: 10.1016/j.spinee.2007.07.389. [DOI] [PubMed] [Google Scholar]
  • 17.Fillion L., Gagnon P., Leblond F., Gélinas C., Savard J., Dupuis R., Duval K., Larochelle M. A brief intervention for fatigue management in breast cancer survivors. Cancer Nursing. 2008;31(2):145–159. doi: 10.1097/01.NCC.0000305698.97625.95. [DOI] [PubMed] [Google Scholar]
  • 18.Scaffidi M., Vulpiani M. C., Vetrano M., Conforti F., Marchetti M. R., Bonifacino A., Marchetti R., Saraceni V. M., Ferretti A. Early rehabilitation reduces the onset of complications in the upper limb following breast cancer surgery. European Journal of Physical and Rehabilitation Medicine. 2012;48(4):601–611. [PubMed] [Google Scholar]
  • 19.Boquiren V. M., Esplen M. J., Wong J., Toner B., Warner E. Exploring the influence of gender-role socialization and objectified body consciousness on body image disturbance in breast cancer survivors. Psycho-Oncology. 2013;22(10):2177–2185. doi: 10.1002/pon.3271. [DOI] [PubMed] [Google Scholar]
  • 20.Green L. W., Kreuter M. W., Deeds S. G., Partridge K. B. Health Education Planning: A Diagnostic Approach. Mountain View, Calif, USA: Mayfield Publishing Company; 1980. [Google Scholar]
  • 21.Yates P., Aranda S., Hargraves M., Mirolo B., Clavarino A., McLachlan S., Skerman H. Randomized controlled trial of an educational intervention for managing fatigue in women receiving adjuvant chemotherapy for early-stage breast cancer. Journal of Clinical Oncology. 2005;23(25):6027–6036. doi: 10.1200/JCO.2005.01.271. [DOI] [PubMed] [Google Scholar]
  • 22.Aaronson N. K., Ahinedzai S., Bergman B., Bullinger M., Cull A., Duez N. J., Filiberti A., Flechtner H., Fleishman S. B., De Haes J. C. J. M., Kaasa S., Klee M., Osoba D., Razavi D., Rofe P. B., Schraub S., Sneemv K., Sullivan M., Takeda F. The European Organization for Research and Treatment of Cancer QLQ-C30: a quality-of-life instrument for use in international clinical trials in oncology. Journal of the National Cancer Institute. 1993;85(5):365–376. doi: 10.1093/jnci/85.5.365. [DOI] [PubMed] [Google Scholar]
  • 23.Fayers P., Aaronson N. K., Bjordal K., Curran D., Groenveld M. EORTC QLQ-C30 Scoring Manual. 2nd. Brussels, Belgium: EORTC; 1999. [Google Scholar]
  • 24.Apolone G., Filiberti A., Cifani S., Ruggiata R., Mosconi P. Evaluation of the EORTC QLQ-C30 questionnaire: a comparison with SF-36 Health Survey in a cohort of Italian long-survival cancer patients. Annals of Oncology. 1998;9(5):549–557. doi: 10.1023/A:1008264412398. [DOI] [PubMed] [Google Scholar]
  • 25.Hamilton M. A rating scale for depression. Journal of Neurology, Neurosurgery, and Psychiatry. 1960;23:56–62. doi: 10.1136/jnnp.23.1.56. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26.Bonaiuti D. Scale di Misura in Riabilitazione. 3rd. Rome, Italy: Societa Editrice Universo; 2011. [Google Scholar]
  • 27.Hamilton M. Handbook of Psychiatric Measures. Washington, DC, USA: APA; 2000. Hamilton rating scale for Depression (Ham-D) pp. 526–528. [Google Scholar]
  • 28.Spielberger G. O. The State-Trait Anxiety Inventory. Palo Alto, Calif, USA: Consulting Psychologists Press; 1970. [Google Scholar]
  • 29.Spielberg C. D., Gorsuch R. L., Lushene R. E. STAI State-Trait Anxiety Inventory, Forma Y. Firenze, Italy: Organizzazioni Speciali; 1989. (edited by L. Pedrabissi and M. Santinello). [Google Scholar]
  • 30.Hudak P. L., Amadio P. C., Bombardier C. Development of an upper extremity outcome measure: the DASH (disabilities of the arm, shoulder and hand). The Upper Extremity Collaborative Group (UECG) American Journal of Industrial Medicine. 1996;29(6):602–608. doi: 10.1002/(SICI)1097-0274(199606)29:6<602::AID-AJIM4>3.0.CO;2-L. [DOI] [PubMed] [Google Scholar]
  • 31.Padua R., Padua L., Ceccarelli E., Romanini E., Zanoli G., Amadio P. C., Campi A. Italian version of the disability of the arm, shoulder and hand (DASH) questionnaire: cross-cultural adaptation and validation. The Journal of Hand Surgery. 2003;28(2):179–186. doi: 10.1016/S0266-7681(02)00303-0. [DOI] [PubMed] [Google Scholar]
  • 32.Speck R. M., Gross C. R., Hormes J. M., Ahmed R. L., Lytle L. A., Hwang W., Schmitz K. H. Changes in the body image and relationship scale following a one-year strength training trial for breast cancer survivors with or at risk for lymphedema. Breast Cancer Research and Treatment. 2010;121(2):421–430. doi: 10.1007/s10549-009-0550-7. [DOI] [PubMed] [Google Scholar]
  • 33.Michael S., Charikleia S., Konstantinos K. Lymphedema and breast cancer: a review of the literature. Breast Cancer. 2011;18(3):174–180. doi: 10.1007/s12282-010-0246-1. [DOI] [PubMed] [Google Scholar]
  • 34.Morone G., Iosa M., Paolucci T., Fusco A., Alcuri R., Spadini E., Saraceni V. M., Paolucci S. Efficacy of perceptive rehabilitation in the treatment of chronic nonspecific low back pain through a new tool: a randomized clinical study. Clinical Rehabilitation. 2012;26(4):339–350. doi: 10.1177/0269215511414443. [DOI] [PubMed] [Google Scholar]
  • 35.Paolucci T., Fusco A., Iosa M., Grasso M. R., Spadini E., Paolucci S., Saraceni V. M., Morone G. The efficacy of a perceptive rehabilitation on postural control in patients with chronic nonspecific low back pain. International Journal of Rehabilitation Research. 2012;35(4):360–366. doi: 10.1097/MRR.0b013e328356427c. [DOI] [PubMed] [Google Scholar]
  • 36.Paolucci T., Morone G., Iosa M., Fusco A., Alcuri R., Matano A., Bureca I., Saraceni V. M., Paolucci S. Psychological features and outcomes of the Back School treatment in patients with chronic non-specific low back pain. A randomized controlled study. European Journal of Physical and Rehabilitation Medicine. 2012;48(2):245–253. [PubMed] [Google Scholar]
  • 37.Kurtzman S. H., Gardner B., Kellner W. S. Rehabilitation of the cancer patient. American Journal of Surgery. 1988;155(6):791–803. doi: 10.1016/S0002-9610(88)80045-X. [DOI] [PubMed] [Google Scholar]
  • 38.Paolucci T., Morone G., Iosa M., Grasso M. R., Buzi E., Zangrando F., Paolucci S., Saraceni V. M., Fusco A. Efficacy of group-adapted physical exercises in reducing back pain in women with postmenopausal osteoporosis. Aging Clinical and Experimental Research. 2014;26(4):395–402. doi: 10.1007/s40520-013-0183-x. [DOI] [PubMed] [Google Scholar]
  • 39.Zhao G., Li C., Li J., Balluz L. S. Physical activity, psychological distress, and receipt of mental healthcare services among cancer survivors. Journal of Cancer Survivorship. 2013;7(1):131–139. doi: 10.1007/s11764-012-0254-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 40.Bragoni M., Broccoli M., Iosa M., et al. Influence of psychologic features on rehabilitation outcomes in patients with subacute stroke trained with robotic-aided walking therapy. American Journal of Physical Medicine and Rehabilitation. 2013;92(10, supplement 2):e16–e25. doi: 10.1097/PHM.0b013e3182a20a34. [DOI] [PubMed] [Google Scholar]
  • 41.Benton M. J., Schlairet M. C., Gibson D. R. Change in quality of life among breast cancer survivors after resistance training: is there an effect of age? Journal of Aging and Physical Activity. 2014;22(2):178–185. doi: 10.1123/japa.2012-0227. [DOI] [PubMed] [Google Scholar]

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