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1.
Article de Anglais | MEDLINE | ID: mdl-33228006

RÉSUMÉ

We studied the determinants of motivation among post-menopausal women enrolled in a two-year diet and physical activity primary prevention randomized trial. Participants were requested to grade the importance attached to changing their lifestyle, their confidence about being able to implement the change, and their willingness to be involved in studies focusing on lifestyle. We used multi-adjusted regression to investigate the association between individual characteristics, study arm, and individual motivation at study entry and end. Participants (n = 234) were highly motivated both at entry and throughout the study. Women with pre-existing healthier eating habits and lifestyles (e.g., high consumption of fruit and vegetables, low red meat consumption, and physically active) were more motivated at entry and over the course of the study. Women assigned to any intervention arm were more motivated than those in the control arm. These findings may help enhance adherence to recommendations and improve effectiveness of community-based health promotion campaigns.


Sujet(s)
Régime alimentaire , Exercice physique , Motivation , Prévention primaire , Sujet âgé , Régime alimentaire/psychologie , Exercice physique/psychologie , Femelle , Humains , Adulte d'âge moyen , Prévention primaire/méthodes , Facteurs temps , Légumes
2.
Support Care Cancer ; 21(9): 2381-6, 2013 Sep.
Article de Anglais | MEDLINE | ID: mdl-23564074

RÉSUMÉ

BACKGROUND: Combining medical and psychological knowledge and accompanying patients in an individualised path, the Oncological Rehabilitation Centre of Florence (CeRiOn) aims at offering effective integrated rehabilitation interventions and at reducing psychological distress in cancer patients. In the present observational study, we measured the psychological distress at baseline and at the end of the completed rehabilitation processes. METHODS: A total number of 627 cancer patients were treated by the psycho-oncological service at CeRiOn in 2007-2010. Among them, 99 (all women) participated in more than or equal to three sessions, were followed up for clinical and life status for at least 1 year and had a formal conclusion of their psychological rehabilitation process. For 98 cases, both a baseline and a follow-up measure of distress, by the Psychological Distress Inventory (PDI) and the Distress Thermometer (DT), were available. RESULTS: Relevant before-after amelioration in this selected group of psychologically, highly suffering cancer patients has been shown. Almost all the patients (except 20%) received both group and individual psychological support. The average rehabilitation process lasted 1.7 years. Average distress evaluation decreased from a baseline of 34.7 to 26.4 (P < 0.001) according to PDI and from 5.9 to 2.2 according to DT (P < 0.001). CONCLUSIONS: On average, quite a long psychological support time was necessary to complete the rehabilitation process. During this period, patients who had a formal conclusion of the psychological support received at CeRiOn showed a significant reduction of their distress.


Sujet(s)
Tumeurs du sein/psychologie , Tumeurs du sein/rééducation et réadaptation , Programme clinique , Centres de rééducation et de réadaptation , Soutien social , Stress psychologique/psychologie , Adaptation psychologique , Adulte , Tumeurs du sein/chirurgie , Assistance , Femelle , Études de suivi , Humains , Adulte d'âge moyen , Récidive tumorale locale/psychologie , Récidive tumorale locale/rééducation et réadaptation , Récidive tumorale locale/chirurgie , Résultat thérapeutique
3.
Epidemiol Prev ; 36(1): 56-8, 2012 Jan.
Article de Italien | MEDLINE | ID: mdl-22418804

RÉSUMÉ

In the short paper we report the results of a workshop on the feasibility to carried out a brief counselling on smoking cessation and physical activity to female smokers attending the Italian National Health System Cervical Cancer Screening Program. The considerations derived from the midwives' experience during the recruitment of women for the SPRINT study, an intervention trial designed in order to verify the effectiveness of a standard counselling intervention on smoking cessation delivered by trained midwives in a gender-specific setting, the outpatient cervical cancer screening visits.


Sujet(s)
Assistance , Mode de vie , Activité motrice , Prévention secondaire , Arrêter de fumer/méthodes , Études de faisabilité , Femelle , Humains
4.
BMC Public Health ; 11: 906, 2011 Dec 07.
Article de Anglais | MEDLINE | ID: mdl-22151834

RÉSUMÉ

BACKGROUND: Gender-specific smoking cessation strategies have rarely been developed. Evidence of effectiveness of physical activity (PA) promotion and intervention in adjunct to smoking cessation programs is not strong. SPRINT study is a randomized controlled trial (RCT) designed to evaluate a counselling intervention on smoking cessation and PA delivered to women attending the Italian National Health System Cervical Cancer Screening Program. This paper presents study design and baseline characteristics of the study population. METHODS/DESIGN: Among women undergoing the Pap examination in three study centres (Florence, Turin, Mantua), participants were randomized to the smoking cessation counselling [S], the smoking cessation + PA counselling [S + PA], or the control [C] groups. The program under evaluation is a standard brief counselling on smoking cessation combined with a brief counselling on increasing PA, and was delivered in 2010. A questionnaire, administered before, after 6 months and 1 year from the intervention, was used to track behavioural changes in tobacco use and PA, and to record cessation rates in participants. DISCUSSION: Out of the 5,657 women undergoing the Pap examination, 1,100 participants (55% of smokers) were randomized in 1 of the 3 study groups (363 in the S, 366 in the S + PA and 371 in the C groups). The three arms did not differ on any demographic, PA, or tobacco-use characteristics. Recruited smokers were older, less educated than non-participant women, more motivated to quit (33% vs.9% in the Preparation stage, p < 0.001), smoked more cigarettes per day (12 vs.9, p < 0.001), and were more likely to have already done 1 or more quit attempts (64% vs.50%, p < 0.001). The approach of SPRINT study appeared suitable to enrol less educated women who usually smoke more and have more difficulties to quit. TRIAL REGISTRATION NUMBER: ISRCTN: ISRCTN52660565.


Sujet(s)
Assistance , Promotion de la santé/méthodes , Activité motrice , Test de Papanicolaou , Infections à papillomavirus/diagnostic , Arrêter de fumer , Frottis vaginaux , Adulte , Attitude envers la santé , Niveau d'instruction , Femelle , Humains , Dépistage de masse , Programmes nationaux de santé , Éducation du patient comme sujet , Évaluation de programme , Classe sociale , Santé des femmes
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