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Intestine manipulation and functionality in patients with intestinal constipation

Intestine manipulation and functionality in patients with intestinal constipation: randomized controlled double blinded clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-3zyq7b
Enrollment
Unknown
Registered
2019-07-31
Start date
2019-07-01
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

Constipation

Interventions

Researchers will evaluate the mobility of the ascending, descending, sigmoid colon, and ilio-cecal sphincter. Next, the mobilization will be performed, in which the patient will be asked to position h
Behavioural
E02.190.599.280

Sponsors

Colegio Brasileiro de Osteopatia
Lead Sponsor
Colegio Brasileiro de Osteopatia
Collaborator

Eligibility

Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria will be adults; of both genders; aged between 18 and 60 year;s and who present a complaint of Chronic Intestinal Constipation (more than 6 months), that fit the definition of Functional Constipation in the Rome Consensus III;

Exclusion criteria

Exclusion criteria: Adults with an incision or tumor in the abdominal region; fractures; rheumatic diseases; acute infectious disease; or impossibility of understanding the proposed evaluations will be excluded.

Design outcomes

Primary

MeasureTime frame
Improvement in symptoms reported by the Scale of Intestinal Symptoms - ESI. 174/5000 This evaluation will be applied before the intervention, immediately after the first session of intestinal manipulation and one week after the fifth session of intestinal manipulation. This instrument measures the report of the intensity of the intestinal symptoms, containing 10 questions, scored from 0 to 4. Question 1 refers to the frequency of evacuation, and questions 2 to 10 are related to intestinal symptoms. The final score of the questionnaire corresponds to the mean of the scores obtained in each question, and reports on a scale from 0 (nonexistent) to 4 (total), the intensity of intestinal symptoms;Improvement of intestinal functionality by the Inventory of Intestinal Functionality - IFI. This evaluation will be applied before the intervention, immediately after the first session of intestinal manipulation and one week after the fifth session of intestinal manipulation. The instrument evaluates intestinal motility with 57 questions related to the presence of nonspecific intestinal symptoms associated with daily events, interpersonal relationships and stress situations. The score for each question is given according to the frequency of the symptoms (0 - never, 1 - few times, 2 - half of the time, 3 - often 4 - always) and its consequences, such as escape from a certain situation or non - of a given task.

Secondary

MeasureTime frame
Improvement in static equilibrium through baropodometry. This evaluation will be applied before the intervention, immediately after the first session of intestinal manipulation and one week after the fifth session of intestinal manipulation. Computerized baropodometry is a simple system that measures the distribution of plantar pressures during the orthostatic position. The Fusyo model (Medcapteurs France S.A.S, France), which has 2000 sensors and a frequency of 40Hz, will be used. This equipment records quantitative data on the pressures at different anatomical points of plantar surface and the anteroposterior and lateral-lateral deviation. For the examination the individual should climb on a pressure platform, barefoot, in an orthostatic position, with the arms along the body, keeping a fixed stare horizontally, with lips closed and jaw relaxed as well as the rest of the body. The duration of the registration will be approximately 20 seconds. The values will be recorded by the program supplied by the manufacturer itself, installed in a microcomputer.;Decreased perception of pain on the spinal processes of the thoracic and lumbar spine through algometry. This evaluation will be applied before the intervention, immediately after the first session of intestinal manipulation and one week after the fifth session of intestinal manipulation. Algometry is a technique that uses quantification through physical stimuli (pressure on the nociceptors) the capacity for painful perception and tolerances. In this study, a digital pressure algometer (model D-200, Instrutherm®) consisting of a rod (probe) with a circular head coated with rubber (area 1cm2) and a display that informs the pressure exerted in Kgf (kilogram force) . Thus, once the tip surface is 1cm2, the readings will be expressed in kg / cm2. The range of the algometer is 0-10 kg with 0.1 kg divisions. The site of measurement of pain through the algometro will be in the spinous processes of the vertebrae of the

Countries

Brazil

Contacts

Public ContactHugo;Lucas Pasin Neto;Villalta Santos

Colegio Brasileiro de Osteopatia;Faculdade de Ciências Médicas da Santa Casa de São Paulo

hugo.pasini@cbosteopatia.com.br;lucasvillalta.s@gmail.com(15)981179143;+55-015-998197899

Outcome results

None listed

Source: REBEC (via WHO ICTRP)