Colorectal cancer, inflammatory bowel disease, Diverticular disease, Chagas Disease, Fournier Syndrome, Perineal trauma abdominoperineal, Ostomy
Conditions
Interventions
Practice of Circular dance moves: Intervention: It will start with an experimental group and one control group.
Experimental Group: (Sample Number 90 individuals)
Intervention period: 12( twelve) weeks
frequency: 02 (twice) a week
duration: 60 (sixty minutes)
Location: Reference Center in Integrative Practices (CERPIS) located at Planaltina, Federal District. Also, the potential individuals to undergo the intervention shall fulfill a questionaire for asses
Other
Sponsors
Universidade de Brasília - UNB
Hospital Regional de Sobradinho
Hospital Regional de Planaltina
Centro de Referência em Práticas Integrativas em Saúde
Eligibility
Age
18 Years to 90 Years
Inclusion criteria
Inclusion criteria: Men and women over the age of eighteen (18) years, intestinal ostomy, without participation in any dance form, showing understanding and conditions for continuing the intervention in CERPIS (Reference Center for Integrative Practices in Health), and who agree to participate in the study by signing the Informed Consent.
Exclusion criteria
Exclusion criteria: Children, adolescents, pregnant women, nursing mothers, bedridden, disabled and other patients deficit. Patients undergoing other alternative techniques for management of quality of life, such as meditaion, Yoga, self massage and other practices defined under the National Programme for Integrative and Complementary practices (PNPIC).
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary outcome measure being considered is the intervention of the practice of dance move that will have a period of 12 intervention (twelve) weeks. Shall be considererd, quantitative changes in the spectrum of the evaluation of perception of quality of life questionnaire (COH-QOL-OQ - City of Hope - Quality of Life Ostomy Questionnaire)), requiring a change of, at least, 5% in the values obtained prior to the intervention as well as when compared to the control group. | — |
Secondary
| Measure | Time frame |
|---|---|
| The secondary outcomes shall consider the changes in the components of the clinical evaluation - which must include the physical exams, the summary and examinations of weight and height as well as BPM ( Beat per minute) , Respiratory frequency, arterial pressure, BMI ( Body MAss Index) and abdominal circunference values. Complementarily, antropometric measures using the Bodystat 1500 device shall be used to estimate Body Fat, Total Weight, Body Water Percentage, Lean Mass and Metabolic Basal Rate. Also, the clinical evaluation shall be enriched by laboratory essays, in serum, as C-Reactive Protein, Fasting Glucose, Lipid Profile and Fractions,Thyroid Stimulating Hormone, Cortisol, Insulin, Parathormone (PTH), Total Triiodothyronine (T3), Total thyroxin (T4), Anti Nuclear Factor. The return of such values into the normality zone shall be considered as proxies for intervention success, assuming statistical significance (p value lower than 0,05). Foremost, the COH-QOL-OQ questionnaire ( City of Hope - Quality of life - Ostomy Questionnaire) shall assess the aforementioned domains: Physical Wellness, Psychological Wellness, Social Wellness, Spiritual Wellness, in order to better know the self perception of quality of life and the interpretations of the biosocial reality of the stomized patients. Changes in que self perception of quality of life, when statistically significant, shall be considered sucess in the intervention. | — |
Countries
Brazil
Contacts
Public ContactCristilene Kimura
Universidade de Brasília - UNB
Outcome results
None listed