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Effects of Osteopathic Manipulative Treatment in women with Intestinal Constipation

Effects of Osteopathic Manipulative Treatment in women with Functional Constipation: pragmatic randomized clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-47nqzj2
Enrollment
Unknown
Registered
2023-07-18
Start date
2023-08-01
Completion date
Unknown
Last updated
2025-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Intestinal Constipation

Interventions

Through the dissemination of social networks, volunteers will be recruited who must meet the following inclusion criteria: be in the age group of 18 to 60 years and presente functional intestinal cons
referred cold pain whit the visual analog pain scale test, range of motion of the lumbar region with the Wells bank and Heart Rate Variability. The data collection of this study will be carried out a
E02.190.599.280

Sponsors

Univerisade Estadual do Oeste do Paraná
Lead Sponsor
Univerisade Estadual do Oeste do Paraná
Collaborator

Eligibility

Sex/Gender
Female
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Women; age range from 18 to 60 years; present functional constipation as mentioned in the ROME III criteria (LONGSTRETH et al., 2006)

Exclusion criteria

Exclusion criteria: Not accepting manipulations; pregnant women; being in the inflammatory phase of gastrointestinal or urinary diseases (kidney stones, appendicitis, colicistitis, peritonitis); presenting metabolic or cardiovascular diseases; having already undergone some surgical procedure on the spinal column or abdominal cavity; having undergone some type of treatment for constipation less than 6 months ago, such as: use of laxative medications and body massages or teas that alter intestinal motility; present contraindications for the Osteopathic techniques to be performed during the collection of the study, these being: recent fracture, osteoporosis and spinal tumor (PANAGOPOULOS et al. , 2015; FERNANDES et al., 2018)

Design outcomes

Primary

MeasureTime frame
We expect to find improvement in heart rate modulation verified by the Polar H10 through heart rate variability analysis. We will observe whether the heart rate curves will behave in the same way before and after the application of the treatment through the Kubios HRV Software in the time and frequency domain

Secondary

MeasureTime frame
We expect to find improvement in functional constipation assessed by the ROMA Criteria III and Constipation Scoring System questionnaires. We will observe the scores of the questionnaires before and after treatment;We expect to find a decrease in pain referred to the lower abdomen area as assessed by the Visual Analog Scale (VAS), we will take into account the analysis of the scale indicated by the patient before and after the treatment, to observe if there is a difference in pain sensation;We expect to find an improvement in the mobility of the lumbar spine evaluated by the Wells bench, through the measurement of the patient's reach. We will take into account the mean and standard deviation of the measurements made by the collections before and after treatment and we will make a comparison between the measurements considering a p<0.05 significant;We expect to observe an improvement in quality of life as assessed by the SF-36 questionnaire, applied before treatment and 45 days after the first intervention. We will take into account the score of the questionnaire to compare the results

Countries

Brazil

Contacts

Public ContactDébora Thomé

Univerisade Estadual do Oeste do Paraná

debora.thome@hotmail.com+55(45)999038460

Outcome results

None listed

Source: REBEC (via WHO ICTRP)