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Improving health-related quality of life in women with breast, blood, and gynaecological Cancer with an eHealth-enabled 12-week lifestyle intervention: the women’s wellness after Cancer program randomised controlled trial



The residual effects of cancer and its treatment can profoundly affect women’s quality of life. This paper presents results from a multisite randomized controlled trial that evaluated the clinical benefits of an e-health enabled health promotion intervention (the Women’s Wellness after Cancer Program or WWACP) on the health-related quality of life of women recovering from cancer treatment.


Overall, 351 women previously treated for breast, blood or gynaecological cancers were randomly allocated to the intervention (WWACP) or usual care arms. The WWACP comprised a structured 12-week program that included online coaching and an interactive iBook that targeted physical activity, healthy diet, stress and menopause management, sexual wellbeing, smoking cessation, alcohol intake and sleep hygiene. Data were collected via a self-completed electronic survey at baseline (t0), 12 weeks (post-intervention, t1) and 24 weeks (to assess sustained behaviour change, t2). The primary outcome, health-related quality of life (HRQoL), was measured using the Short Form Health Survey (SF-36).


Following the 12-week lifestyle program, intervention group participants reported statistically significant improvements in general health, bodily pain, vitality, and global physical and mental health scores. Improvements were also noted in the control group across several HRQoL domains, though the magnitude of change was less.


The WWACP was associated with improved HRQoL in women previously treated for blood, breast, and gynaecological cancers. Given how the synergy of different lifestyle factors influence health behaviour, interventions accounting for the reciprocity of multiple health behaviours like the WWACP, have real potential for immediate and sustainable change.

Trial registration

The protocol for this randomised controlled trial was submitted to the Australian and New Zealand Clinical Trials Registry on 15/07/2014 and approved on 28/07/2014 (ACTRN12614000800628).

Peer Review reports


Aging populations and the increased prevalence of other cancer risk factors have led to an increased incidence of cancer in women globally [1]. According to the International Agency for Research on Cancer (IARC), more than 4.2 million women worldwide were diagnosed with breast, blood, or gynaecological cancers in 2020, accounting for one-third of new cancers during that period [1, 2]. Cancer incidence in Australia reflects global trends. In 2019, incident cases of breast, blood and gynaecological cancer were estimated to be approximately 32,000 [3]. While cancer rates continue to grow, 5-year survival has also increased. In 2016 it was estimated that two-thirds of Australian women previously diagnosed with cancer were currently living with its long-term effects [3].

Cancer treatments often leave women with a range of residual physical and psychological side effects including neuropathy [4], fatigue, cognitive disruption [5], lymphoedema, osteoporosis [6, 7], treatment-induced menopausal symptoms and psychological distress [8]. These residual effects can compromise women’s ability to sustain healthy lifestyle behaviours [9] and further heighten their risk of treatment-related chronic disease [10]. These residual treatment effects can also profoundly undermine women’s quality of life and physical functioning as they move into older adulthood.

Comprehensive cancer rehabilitation can reduce symptom burden and health service utilisation, whilst generally improving health-related quality of life (HRQOL) [11, 12]. However, for maximum benefits it is critical that supportive interventions address concurrent and overlapping risk factors [7] (not just one risk factor) and also enhance women’s capacity to self-manage any issues in the longer term. This synergistic approach enhances intervention effectiveness and longer-term sustainability [13,14,15].

While there is international recognition that comprehensive recovery care is needed, services in Australia are rarely resourced to deliver this [7, 16,17,18]. Once women have completed active treatment, opportunities to access education and support to help them optimise health behaviours are limited [17]. This is further compounded by remoteness, with almost one-third of Australian women living outside major metropolitan areas, and for these women, their restricted access to health services is associated with poorer health outcomes [19]. Thus, while women are living longer after cancer, the opportunity for better recovery is limited, depriving women of the ability to maximise their health potential.

The Women’s Wellness after Cancer Program (WWACP) is a multimodal, individualised, and digitised lifestyle intervention that was designed to address these gaps [20]. The WWACP capitalised on women’s propensity for lifestyle change at the completion of active treatment for breast, gynaecological, or blood cancers. The program, created for the post-acute cancer care milieu, aimed to enhance HRQOL, decrease the late effects of cancer treatment, and reduce chronic disease risk factors in this population. We used an e-health platform to maximise opportunities for engagement while reducing the potential barriers associated with geography, transportation, cost, and time. The primary objective of the study was to explore the effect of the WWACP on the HRQOL of women diagnosed with cancers associated with treatment-induced menopause. It was hypothesised that, compared to controls, women enrolled in the WWACP would report better HRQOL at the end of intervention (Week 12), which would persist at Week 24.


Study design

This multi-centre, single-blinded, randomised controlled 12-week trial included five hospitals in three Australian states, consumer groups, and supportive cancer care services serving women across Australia. The primary aim of this study was to test the efficacy of a multimodal, digitised lifestyle intervention on HRQOL of women treated for cancer. After baseline assessment, three hundred and fifty-one women previously treated for breast, blood or gynaecological cancer were randomly assigned to either an intervention or usual care arm using permuted-block randomisation. A computer-generated allocation sequence [21, 22] using blocks of varying length was developed by the trial statistician, and randomization was performed by the trial coordinator, who logged into a secure server to obtain the next allocation. While blinding of participants was not possible, the trial statistician and study staff (except for the trial coordinator and those who delivered the intervention) were unaware of group allocation.

Data were collected from participants via online questionnaires and virtual consultations at three time points, baseline (t0), 12 weeks (t1) and 24 weeks (t2). The protocol for this trial was submitted to the Australian and New Zealand Clinical Trials Registry on 15/07/2014 (ACTRN12614000800628). Complete protocol details including the funding source, ethical approvals, the sampling and recruitment, randomisation procedure, intervention content and delivery mode, primary and secondary endpoints, and approach to data analysis are described elsewhere [20]. However, some deviations from the reported protocol in relation to time since diagnosis should be noted, with around 22% (n = 62) of women enrolled in the study being diagnosed with cancer more than 2 years earlier.

Study population

Women who had completed treatment for breast, blood, or gynaecological cancer who were proficient in English, and who had access to an Apple computer and/or iPad were invited to participate in the study. Most participants reported having combined cancer treatment (55.9% reported surgery, chemotherapy + radiation; 20.6% reported surgery + radiation; 12.5% reported surgery + chemotherapy), 76.5% of women’s treatments included hormone therapy, and a smaller proportion reported a single modality treatment (> 1% had radiation therapy and 10% of participants reported having surgery). Women with metastatic or advanced cancer, inoperable or active loco-regional disease, or on maintenance chemotherapy for blood cancers were not eligible to participate in this study (they are the focus of future intervention studies).


The WWACP was underpinned by Social Cognitive Theory, an approach that recognises the importance of reciprocal determinism and behavioural capacity on self-efficacy for health behaviour change [23]. The program supported women to make incremental and feasible changes to less healthy lifestyle behaviours, enhancing their self-efficacy and developing and sustaining healthy lifestyle habits. The intervention was delivered via an e-enabled platform including an iBook and virtual health consultations (detailed previously [20]). Briefly, the structured 12-week intervention comprised a website with educational podcasts and exercise planners; an interactive iBook with practical information to support adoption and maintenance of healthy lifestyle behaviours and tracking of health behaviour changes goals; three virtual consultations with a registered nurse to support the development of realistic and achievable health goals and explore the strategies to enhance women’s self-efficacy for health behaviour change.

Primary endpoint

Initially, we measured HRQoL using two instruments, the Functional Assessment of Cancer Therapy—General (FACT—G) scale [24] and the Short Form Health Survey (SF-36) [25]. However, while the FACT—G is a robust and well-validated measure for evaluating HRQoL among patients receiving cancer treatment [24, 26, 27], its responsiveness in ‘longer-term’ after cancer groups in largely unknown [26]. As almost one-quarter of women in this study were more than 2 years since diagnosis, and the focus of the FACT—G instrument is on measuring cancer-specific concerns rather than broader HRQoL concerns reported in after-cancer populations [26], this paper reports SF-36 data only.

The SF-36 is a 36-item self-reported generic health measurement that examines eight dimensions of health, including physical functioning (PF), role limitations due to physical health (RP), bodily pain (BP), general health (GH), vitality (VT), social functioning (SF), role limitations due to emotional health (RE), and mental health (MH). The instrument also provides two composite measures for mental (Mental Component Summary, MCS) and physical (Physical Health Component, PCS) functioning and wellbeing [25]. The SF-36 is scored using QualityMetric Health Outcomes™ Scoring Software (QualityMetric, Inc., Lincoln, RI) to form standardised 100-point scales, with higher scores denoting better physical and mental functioning [25].This instrument has been extensively used in a variety of clinical and community populations, including women after cancer treatment, with consistently good reliability and validity [25, 28].

Statistical analysis

Statistical analyses were performed using Statistical Package for the Social Sciences, version 23 (SPSS, Inc., Chicago, IL) and STATA 11 (StataCorp, Inc., College Station, TX). SPSS was used for generating descriptive (are expressed as counts and percentages, mean, and standard deviation (SD) and bivariate statistics (t-tests), and one-way Analysis of Covariance (ANCOVA). Statistical significance set at α = 0.05.

To assess the potential impact of attrition on results, two separate analyses, per-protocol (PP) and intent-to-treat (ITT), were performed in SPSS [29]. ITT analysis imputed outcome data for 12-weeks (t1) and 24-weeks (t2) using the last-observation-carried-forward method of imputation.

Incomplete baseline scores were noted in several instances with five of the women enrolled in the study did not provide sufficient baseline data to estimate the primary endpoints and were excluded from the analysis (discussed further in Fig. 1 and Table S1). Withdrawal from the study was greatest among participants who completed the online questionnaire but who did not also want to provide further biophysical data via a virtual consultation. The characteristics of the 68 women lost to follow-up (LTFU) during this period were compared with women who continued in the study (see Table S2). Findings suggested that women who withdrew were more likely to be in the lower income brackets (p = 0.01), born in Australia (p < 0.01), but were more likely to speak a language other than English at home (p = 0.03).

Fig. 1
figure 1

Consort diagram of the Women’s Wellness after Cancer Program (WWACP) clinical trial. All participants provided baseline data (t0) before being randomised to either the intervention or standard care group. The intervention group completed a 12-week e-enabled lifestyle intervention while the standard care group received general information only. Data were collected from all participants at 12- (t1) and 24- weeks (t2)

Within-group change in HRQoL scores over the intervention period were assessed using split sample paired t-tests and Cohen’s d. Effect size was derived using an online calculator that accounted for correlations in the outcome variable over time (more information can be obtained at, which suggested that d = 0.2, 0.5 or 0.8 were equivalent to a small, moderate, and large effect respectively [30].

Individual- and group-level changes in HRQoL across the trial period using linear mixed-effect models (LMM) with an autoregressive residual variance–covariance structure (AR 1) [31] were examined in STATA. This structure was chosen because of the homogeneous variances, decreasing correlations with distance (t0, t1, t2), and the most favourable fit statistic (i.e., the smallest Akaike Information Criterion [AIC] value). To determine model fit, AIC was used in addition to a likelihood ratio chi-square test (LR test). The LR test statistic generates a chi-squared value which, if statistically significant, suggests that the less restrictive model (i.e., the random intercept and slope model) is significantly better than the random intercept only (more restrictive) model.


A total of 798 patients were assessed for eligibility for the study, of whom 351 consented to participate and were randomised following baseline data collection. Among those who commenced the trial, 18 women from the intervention group and 16 women from the control group did not provide data at 12 weeks. A further 12 women were unavailable at 24 weeks (3 intervention participants and 9 control participants). Figure 1 provides an overview of recruitment and flow through the study.

Table 1 details the sociodemographic characteristics or cancer variables of study participants at baseline. The average age of participants was 53 years (SD = 8.8) and almost all had been diagnosed with breast cancer (94.7%) around 19 months (SD = 13.4) before commencing the study. Three quarters were married (76.9%) with a small number reporting being separated or divorced (11.3%), widowed (2.6%) or single (9.2%). Over half reported having a university degree (57.5%), around one-quarter (22.8%) had a technical certificate or diploma and a small proportion of the sample had either a junior (≤ Year 10, 9.0%) or senior (Year 12, 10.7%) certificate. Most of the sample were employed in either a full- or part- time capacity (47.8% and 38.2% respectively) before cancer diagnosis and two-thirds (64.6%) reported a gross household income over $80,000 AUD.

Table 1 Baseline characteristics of women of the study samplea

Both between-group differences, and within-group changes, in SF-36 domain and composite scores were examined using per-protocol (PP) and intent-to-treat (ITT) analyses. Results suggested that while the magnitude of difference was reduced in some instances in the ITT analysis, all differences remained significant and therefore per-protocol results are presented here (ITT analyses are presented in Tables S3 and S4). Between-group changes in HRQoL scores are presented in Table 2. Following adjustment for baseline scores, a 3-point improvement in role limitations due to physical health (95% CI 0.11 – 5.66, p = 0.03) and 2-point improvement in vitality (95% CI 0.36 – 4.13, p = 0.02) was noted at 12-weeks and these changes were sustained at 24-weeks F(1, 238) = 4.41, p = 0.04 and F(1, 231) = 4.20, p = 0.04 respectively). Similar improvements were noted for bodily pain and PCS scores at 12-weeks (F(1, 241) = 5.11, p = 0.02; F(1, 239) = 7.34, p =  < 0.01) though the magnitude of this improvement was reduced at 24-weeks. In contrast, both mental health and general health domain scores showed little change at 12-weeks but a 2-point improvement at 24-weeks (95% CI 0.41 – 4.16, p = 0.02 and 95% CI 0.54 – 4.20, p = 0.01 respectively). Finally, control group participants reported an average 3.78-point improvement improvements in role limitations due to emotional health at 12-weeks (95% CI 0.98 – 5.78, p < 0.01) though this difference was no longer significant at 24-weeks. The results are provided in detail in Table 2.

Table 2 Between-group differences in SF-36 domain and composite summary scores of study participantsa

Within-group changes were also examined over time (Table 3). Overall, women in the intervention group reported modest improvements in many HRQoL measures at 12 weeks and in many instances these improvements were sustained at 24 weeks. For example, a moderate effect was seen in role limitations due to physical health (RP, d = 0.45), social functioning (SF, d = 0.40), and vitality (VT, d = 0.37) and these improvements were sustained at follow-up. Moreover, while MH scores decreased at 12 weeks, significant improvements were noted at 24 weeks (Mchanget1 = 2.7, t(116) = 3.63, p < 0.01; Mchanget2 = -8.3, t(113) = -13.65, p < 0.01). This was also evident in the large effect in mental component summary (MCS) scores at 24 weeks (d = 0.63). Similar trends were also detected in the RP, SF, and MH scores of participants in the control group except for role limitations due to emotional health (RE). While women in the intervention group noted little change in RE scores, women in the control group reported a moderate effect at 12 weeks (d = 0.42).

Table 3 Within-group changes in SF-36 domain and composite summary scores over time using per protocol analysisa

Linear mixed effect models (LMM) examined within-group changes, and between-group differences, in health-related quality of life variables over the intervention period. Table 4 shows the results of the best fitting models for the SF-36 domain sub-scales and composite summary scores, while comparative fit statistics are presented in the online supplementary materials (see Table S5). Overall, the less restrictive model (i.e., the random intercept and slope model) provided the best fit for the data, with 25–64% of the variance in HRQoL scores attributable to differences between individuals (RP, τ = 0.251; PCS, τ = 0.370; PF, τ = 0.395; SF, τ = 0.512; MH, τ = 0.635; MCS, τ = 0.524).

Table 4 Best fitting linear mixed effect model for adjusted SF-36 domain and composite summary scoresa

Over the intervention period, some general improvements in HRQoL were noted for both the intervention and control group. More specifically, both groups reported significant improvements in role functioning (PF), role limitations due to physical health (RP), and social functioning (SF) domains (p < 0.01 for all). Similar trends were also seen in physical and mental component summary (PCS and MCS) scores, although the magnitude of improvement was smaller.

In contrast, the intervention group reported a significant reduction in limitations associated with bodily pain at Time 1  = 2.09, SE = 0.73, p < 0.01) and improvements in general health at Time 2 (β = 2.09, SE = 0.95, p = 0.02) compared to the control group. For both bodily pain and general health domains, around half of the variance in scores was associated with individual difference (ρ = 0.490 and ρ = 0.618 respectively).

Vitality improved in both groups. In the intervention group an average 3.16- and 3.28-point increase in vitality was detected at Times 1 and 2 respectively. The control group also reported general increases over the same period, albeit to a lesser extent (t2, β = 1.68, SE = 0.77, p = 0.03). Changes in the mental health domain scores were also reported. Notably, at Time 1, significant decrements in mental health scores were detected among participants in both the intervention (β = -2.73, SE = 0.69, p < 0.01) and control (β = -4.06, SE = 0.68, p < 0.01) group. At Time 2 however, these decrements were no longer present, with both groups reporting increases in summary mental health scores. While both groups reported improvements, the magnitude of change differed. The intervention group reported better overall mental health scores at Time 2 compared with control group participants (β = 5.24, SE = 0.71, p < 0.01; β = 3.14, SE = 0.72, p < 0.01 respectively). Linear predictors for all domain scores and component summary scores are presented in Figs. 2 and 3.

Fig. 2
figure 2

Change over time in SF-36 domain scores

Fig. 3
figure 3

Change over time in PCS and MCS scores


The completion of acute cancer treatment is a time of increased vulnerability, as women look for ways to mitigate the risk of cancer recurrence [32, 33] and recover from the effects of treatment. Yet cancer services are necessarily acuity focused. Human and financial resource constraints restrict their capacity to provide the comprehensive recovery care that could optimise women’s health and wellbeing once they complete intensive treatment [7, 16,17,18]. This multimodal lifestyle intervention was designed to capitalise on this period of heightened receptivity to lifestyle changes, thereby maximising the uptake of healthy behaviours in women after cancer treatment in the absence of other services.

Our results indicate improvements in many HRQoL domains and in component summary scores. Particularly notable were the improvements in general health and bodily pain, vitality, mental health, and global physical and mental health summary scores among women in the intervention group. While improvements in some of these domains (i.e., VT, MH, MCS, PCS) were also detected in the control group, the magnitude of effect in the intervention group was almost double that reported by control group participants. Previous lifestyle interventions in women after cancer have also shown less fatigue, improved HRQoL, and better quality of sleep in the intervention group compared with controls [34, 35]. Taken together, this suggests that lifestyle interventions can provide non-pharmacologic recovery support that optimises quality of life and reduces symptom burden in women previously treated for cancer.

Quality of life, the primary outcome of this study, was identified in our scoping work with the target group as the most important outcome to them [36]. In the exploratory work undertaken to develop the WWACP, participants emphasised that quality of life is not a single factor, it is multidimensional [36]. They also clearly described how the health behaviours that influenced quality of life worked in synergy and operated across physical, emotional, and social domains [36]. In women treated for cancer, healthy behaviours such as good nutrition and physical activity interact constantly in daily life with each other and with psychosocial factors like emotional distress, sleep quality and fear of recurrence. Hence, the WWACP was designed as a bundled intervention to account for the complexity of health behaviour within the context of each participant’s sociocultural milieu and individual goals for wellbeing. This lifestyle intervention accounted for the reciprocity of these factors and as demonstrated in our results, yielded an immediate and sustainable quality of life benefit. Interventions that compartmentalise rather than synergise health behaviours, and which are not underpinned by strong elements of psychosocial support and self-management, often have good results at the end of the intervention period—but these results are rarely sustained at follow-up [13,14,15, 37]). This observation is reinforced by others who have demonstrated continued adherence and positive patient experiences from multidimensional interventions for weight, diet, and exercise in women with breast cancer [37].

This study has several limitations that should be noted when interpreting the findings. Like many RCTs, selection bias (motivated individuals enrolling in lifestyle intervention) and attrition might have affected the representativeness of the sample. In this study, the largest proportion of women lost to follow-up (LTFU) occurred between randomisation and commencing the study. Excess participant burden associated with the length of the questionnaire and the dual modes of data collection might explain the 20% attrition at this time, though we do not believe it impacted the study outcomes. This study also relied on self-report which is associated with an increased risk of response bias due to the misinterpretation of questions and social-desirability bias even if the survey was de-identified [38]. To minimise the response bias, standard and validated data collection tools were used, and trained data collectors were employed. Finally, most participants were treated for breast cancer, so we hesitate to generalise these findings to women with other cancers. Future research should explore the way in which the core elements of the program can be applied to other cancer groups.

Despite these limitations, this study addresses an unmet need for many women whose cancer-related health effects, while potentially deleterious to their quality of life, are frequently amenable to lifestyle modification. As such, programs like the WWACP have the potential to optimize health by focussing on effective symptom management, preventing late effects, reducing co-morbid conditions, and general health promotion [39]. Moreover, the use of an interactive eHealth platform to deliver a real-time, dynamic, and technology-assisted intervention [40] can enhance patient engagement and capacity for self-management while reducing accessibility barriers faced by many vulnerable populations.


This study demonstrated the effectiveness of a multidimensional digitised lifestyle intervention for the improvement of quality of life among women previously treated for blood, breast, and gynaecological cancers. The intervention employed multiple strategies for tailoring the intervention for individuals, integrating feedback and support mechanisms, and adopting theory-based behaviour change models. The complex and synergistic effects of many modifiable health behaviours emphasise the need for bundled health behaviour interventions to optimise women’s health and wellbeing after completion of active cancer treatment.

Availability of data and materials

The datasets generated and/or analysed during the current study are not publicly available but are available from the corresponding author on reasonable request.



Women’s Wellness After Cancer Program


Health-related quality of life


Randomized controlled trial


International Agency for Research on Cancer


Short Form Health Survey


Functional Assessment of Cancer Therapy-General


Physical functioning


Role limitations due to physical health


Bodily pain


General health




Social functioning


Role limitations due to emotional health


Mental health


Mental Component Summary


Physical Health Component


Statistical Package for the Social Sciences






Lost to follow-up


Linear mixed-effects models




Akaike Information Criterion


Likelihood ratio


National Health and Medical Research Council


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Participating centres: Queensland University of Technology, Brisbane, Australia; University of Notre Dame, Freemantle, Australia; Peter MacCallum Cancer Institute, Melbourne, Australia; Royal Prince Alfred Hospital, Camperdown, Australia; St John of God Murdoch Hospital, Perth, Australia; Wesley Hospital, Brisbane, Australia; Royal Brisbane and Women’s Hospital, Brisbane, Australia; Princess Alexandra Hospital, Brisbane, Australia.

Acknowledgement and sincere thanks to the women who are enrolled in this study.


Funding for this research was received from the National Health and Medical Research Council (NHMRC) Partnership Projects Grant Application (APP1056856).

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Correspondence to Charrlotte Seib or Debra Anderson.

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Ethics approval and consent to participate

The protocol for this randomised controlled trial was registered with the Australian and New Zealand Clinical Trials Registry ACTRN12614000800628 on 28/07/2014. This intervention was performed in accordance with the Declaration of Helsinki and received Cross Institutional Ethical Approval (Australian ethics number: AU/1/E883118) and approvals from all participating sites (Queensland University of Technology, 1300000335; Metro South Health, HREC/13/QPAH/438; Sydney Local Health District, HREC/13/RPAH/366; Saint John of God Health Care, 650; UnitingCare, 1318). Written informed consent was provided by all women prior to enrolment.

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The authors declare that they have no competing interests.

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Supplementary Information

Additional file 1: Table S1.

Missing data and the ability to estimate primary endpoints. Table S2. Sample characteristics by baseline data completiona. Table S3. Between-group differences in SF-36 domain and total scores using intent-to-treat analysis. Table S4. Within-group changes in SF-36 domain and composite summary scores over time using intent-to-treat analysisa. Table S5. Comparisons of model fit for SF-36 data.

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Seib, C., Anderson, D., McGuire, A. et al. Improving health-related quality of life in women with breast, blood, and gynaecological Cancer with an eHealth-enabled 12-week lifestyle intervention: the women’s wellness after Cancer program randomised controlled trial. BMC Cancer 22, 747 (2022).

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  • Cancer
  • Women
  • Health-related quality of life
  • Health behaviour
  • Intervention