Central Nervous System Injury Clinical Trial
Official title:
Neurogenic Bowel Dysfunction: Evaluation of the Effects of Osteopathic Manipulative Treatment in People With Central Nervous System Injury
People affected central nervous system (CNS) diseases often suffer from neurogenic bowel
dysfunction (NBD) that causes a reduction in the quality of life and participation in social
life. Although some conservative approaches exist to treat NBD, none has shown to be
effective in managing this complex condition. Osteopathic manipulative treatment (OMT) has
shown to be efficient in CNS diseases such as epilepsy and migraine.
This randomised trial aims at evaluating the efficacy of osteopathic manipulative treatment
(OMT) in supporting the management of NBD. The research will be conducted at the outpatient
service of Neuro-Urology / Spinal Unit of the Città della Salute e della Scienza Hospital of
Torino.
A sample of 62 participants will be divided into two groups: standard (nursing intervention)
and experimental (nursing intervention and OMT). A neuro-urologist will determine the
eligibility for the study. The outcomes will include self-reported and instrumental measures
that will be evaluated in 3 times (before, at the end of the intervention and the follow- up
three months).
The protocol has been approved by the Ethics Committee of the Città della Salute e della
Scienza Hospital of Torino on 15.04.2019, protocol number 0040534. The standard intervention
has been scheduled for 28.10.2019.
Status | Recruiting |
Enrollment | 70 |
Est. completion date | October 1, 2022 |
Est. primary completion date | October 30, 2020 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - neurogenic bowel dysfunction secondary to acquired disease of the central nervous system - Neurogenic Bowel Dysfunction Score (NBDS) between 6 and 30 Exclusion Criteria: - previous dysfunctional conditions or organic diseases affecting the bowel tract that are pre-existing at neurological diagnosis - patients with an NBDS score lower than 6 (very mild bowel dysfunction) and above 30 (very severe neurogenic bowel dysfunction) - ostomy condition (ileus and colon) - psychiatric patients - presence of cognitive disorders - female patients with proven, or even doubtful, pregnancy status. |
Country | Name | City | State |
---|---|---|---|
Italy | Silvia Mozzone | Vezza d'Alba | CN |
Lead Sponsor | Collaborator |
---|---|
University of Turin, Italy | Azienda Ospedaliera Città della Salute e della Scienza di Torino, SOMA Istituto Osteopatia Milano |
Italy,
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Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Neurogenic bowel dysfunction score (NBDS) | self-reported questionnaire. The Neurogenic Bowel Dysfunction Score is a 10-item questionnaire covering frequency of bowel movements, headache, perspiration or discomfort during defaecation; medication for constipation or faecal incontinence; time spent on defaecation; frequency of digital stimulation or evacuation; frequency of faecal incontinence; flatus; and perianal skin problems. It ranges between 0 and 47; lower scores indicate a better bowel function, while a score over 14 is considered to be an index of severe bowel dysfunction. Score 0-6 Very low 7-9 Low 10-13 Moderate 14 or more Severe The hypothesis of treatment efficacy is supported by the observation of a difference between the groups in the NBDS score. |
- Pre-treatment - Immediately after the treatment - Follow-up at three months after the end of the treatment | |
Secondary | Quality of Life Short Form-36 (SF-36) Questionnaire | self-reported questionnaire. This questionnaire was developed in 1992 to be applied in all health conditions and detect fundamental human values that describe health concepts significant to a person's functional status and wellbeing. It consists of 36 self-administered questions covering eight main domains (vitality, physical functioning, bodily pain, general health, physical role functioning, emotional role functioning, social role functioning, and mental health) represented on a 0-100 scale; a lower score indicates lower quality of life with significant impairments in the specific domain. Higher scores indicate better quality of life in the different domains. | - Pre-treatment - Immediately after the treatment - Follow-up at three months after the end of the treatment | |
Secondary | Bowel transit time | Bowel transit time is a non - invasive diagnostic rx. The exam involves the assumption of radiopaque markers of about two or three millimeters each for six consecutive days and the execution of a single radiograph of the abdomen on the seventh day. | - Pre-treatment - Follow-up at three months after the end of the treatment |
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