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The aim of the WELL-DONE! Study is to co-design, using different professional figures (midwives, psychologists, master's degree in motor science) but also taking into consideration the pregnant women's point of view, an intervention of adapted physical activity for pregnant women, included in the birth accompaniment courses and conducted by midwives, and to evaluate its effectiveness in terms of quality of life, well-being, levels of physical activity and satisfaction with respect to the proposed intervention.
The primary objective is the evaluation of an integrated, co-designed intervention of adapted physical activity, included in the birth accompaniment courses, in order to improve the quality of life of pregnant women.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Experimental Group | Experimental | The Experimental Group will be involved in 1 weekly session of adapted physical activity lasting 1 hour for 6 weeks within the normal cycle of accompanying birth meetings provided by the University Hospital of Bologna. |
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| Control Group | No Intervention | The control group is expected to participate in 6 birth accompaniment meetings held online, 1 hour of which will be dedicated to the topic of exercise and physical activity recommendations in pregnancy. |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Adapted physical activity | Other | Participants in the experimental group will undergo the adapted physical activity program that will be co-designed during phase I of the study. The 6-week program is aimed at improving the quality of life; increase the physical activity levels according to recommended guidelines; improving body awareness through an educational component; maintain and ameliorate the previous functions (for women previously active) and build the exercise background for sedentary women; increase physical fitness and functional capacity. |
| Measure | Description | Time Frame |
|---|---|---|
| Change in Women's Quality of Life | 12-Item Short-Form Health Survey (SF-12 Questionnaire) | Baseline (T1); after 6 weeks of intervention (T2); 3 months after childbirth (T3) |
| Measure | Description | Time Frame |
|---|---|---|
| Change in Physical activity levels | Pregnancy Physical Activity Questionnaire (PPAQ) | Baseline (T1); follow-up after 6 weeks (T2); 3 months after childbirth (T3) |
| Change in Physical Performance |
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Inclusion Criteria:
Exclusion Criteria:
Alterations in communication skills and / or sensory functions so severe as to make it impossible to understand and / or execute the instructions given by the trainer (dementia, aphasia, blindness, deafness);
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Dila Parma | Contact | +39 3313571212 | facmed.cdlostetricia@unibo.it |
| Name | Affiliation | Role |
|---|---|---|
| Dila Parma | University of Bologna, Department of Medical and Surgical Sciences | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Corso di Laurea in Ostetricia - Scuola di Medicina e Chirurgia Alma Mater Studiorum - Università di Bologna | Recruiting | Bologna | 40138 | Italy |
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|
Six minutes walking distance; Sit to stand test
| Baseline (T1); after 6 weeks of intervention (T2); 3 months after childbirth (T3) |