Multiple SclerosisSTAR-QNCT04996186
Symptoms and Treatment Assessment of Ano-Rectal Disorders in Multiple Sclerosis Patients : STAR-Q
An observational study of Multiple Sclerosis and Constipation, run by Pierre and Marie Curie University at 1 site in France.
Trial summary
Multiple sclerosis (MS) is known to cause urinary disorders, sexual and bowel dysfunction. Urinary symptoms due to MS are well known and profit of multiple questionnaire or tool developed in MS patients. Prevalence of bowel disorders in MS is difficult to assess. Some studies up to 70% bowel disorders in MS patients. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Multiple Sclerosis, Constipation, Fecal Incontinence
- What is being tested?
- Clinical interviews
- How many people
- 200 participants
- Where
- 1 siteFrance
- Study dates
- 1 Jun 2019to 30 Apr 2021
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Study population: Patients consulting or hospitalized in a rehabilitation center or in a neuro-urology center
Who may be able to join
- Patients with multiple sclerosis diagnosed on the 2017 revised McDonald's criteria
- over 18 years old
Who cannot join
- inability to read and to understand the questions
- recent relapse of multiple sclerosis
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Symptoms and Treatment Assessment of Ano-Rectal Disorders in Multiple Sclerosis Patients : STAR-Q (STAR Questionnaire): Validation of a New Tool to Better Explore and Manage Bowel Dysfunction.
Multiple sclerosis (MS) is known to cause urinary disorders, sexual and bowel dysfunction. Urinary symptoms due to MS are well known and profit of multiple questionnaire or tool developed in MS patients.
Prevalence of bowel disorders in MS is difficult to assess. Some studies up to 70% bowel disorders in MS patients. Constipation and fecal incontinence are the two main symptoms in neurogenic bowel dysfunction and frequently coexist in this population, generally in association with urinary disorders.
Read more
Because of the high prevalence of bowel disorders their and the major impact on the quality of life of patients with Multiple sclerosis (PwMS) , and the cross-talk bladder-rectum (persistence of anorectal dysfunction leading to poor neurogenic bladder control) assessment of bowel disorders in MS is necessary. But this evaluation is difficult as no specific score exist. The neurogenic Bowel Dysfunction score (NBD) is often used. The NBD was developed and validated for spinal cord injury (SCI) population but not for PwMS MS. Yet NBD is often used in research for all neurologic patients despite its lack of sensibility in various neurogenic population other than spinal cord injury patient. As recommended in a Cochrane revue in 2014, there is a need of a specific evaluation for bowel symptoms in neurogenic population, especially for PwMS.
The aim of the study was to create and validate a new multidimensional questionnaire to assess bowel dysfunction and impact on quality of life in patients with MS.
The investigators conducted a prospective multicenter study (8 centers) between June 2019 to April 2021. This study was developed in 3 steps. First step was literature review and qualitative interview. Then the second step was the feasibility study to evaluate comprehension, acceptability of the different items. The last part of the study was the validation study of the questionnaire. This part of the study was performed between June2020 and April 2021. Validation study allowed to determine the psychometric properties of the new tool.
Patients aged over 18 years with multiple sclerosis diagnosed on the 2017 revised McDonald's criteria were included. Patients not able to read or understand the objectives and procedures for conducting the protocol and patient who had a recent relapse of MS were excluded.
Read the detailed description
Multiple sclerosis (MS) is an autoimmune autoimmune central nervous system (CNS) disorder characterized by demyelinisation and central neurologic damage. MS is the first cause of disability in young adults and affects 2.8 million people in the world.
Multiple sclerosis (MS) is known to cause urinary disorders, sexual and bowel dysfunction. Urinary symptoms due to MS are well known and profit of multiple questionnaire or tool developed in MS patients.
Prevalence of bowel disorders in MS is difficult to assess. Some studies up to 70% bowel disorders in MS patients. Constipation and fecal incontinence are the two main symptoms in neurogenic bowel dysfunction and frequently coexist in this population, generally in association with urinary disorders. Chronic constipation and fecal incontinence were defined by Rome IV criteria. According to these criteria, constipation is a bowel disorder in which symptoms of difficult, infrequent, or incomplete defecation predominate for at least 3 months and fecal incontinence is defined as the recurrent uncontrolled passage of fecal material for at least 3 months.
Moreover, neurogenic bowel dysfunction has a real impact on quality of life and can cause social isolation.
Because of the high prevalence of bowel disorders their and the major impact on the quality of life of patients with Multiple sclerosis (PwMS) , and the cross-talk bladder-rectum (persistence of anorectal dysfunction leading to poor neurogenic bladder control) assessment of bowel disorders in MS is necessary. But this evaluation is difficult as no specific score exist. The neurogenic Bowel Dysfunction score (NBD) is often used. The NBD was developed and validated for spinal cord injury (SCI) population but not for PwMS MS. Yet NBD is often used in research for all neurologic patients despite its lack of sensibility in various neurogenic population other than spinal cord injury patient. As recommended in a Cochrane revue in 2014, there is a need of a specific evaluation for bowel symptoms in neurogenic population, especially for PwMS.
The aim of the study was to create and validate a new multidimensional questionnaire to assess bowel dysfunction and impact on quality of life in patients with MS.
The investigators conducted a prospective multicenter study (8 centers) between June 2019 to April 2021. This study was developed in 3 steps. First step was literature review and qualitative interview. Then the second step was the feasibility study to evaluate comprehension, acceptability of the different items. The last part of the study was the validation study of the questionnaire. All these phases allowed a full psychometric validation of the questionnaire.
Patients aged over 18 years with multiple sclerosis diagnosed on the 2017 revised McDonald's criteria were included. Patients not able to read or understand the objectives and procedures for conducting the protocol and patient who had a recent relapse of MS were excluded.
Step 1: literature review and qualitative interview. The investigators conducted a review of literature on Pubmed to know all the existing questionnaires or tools developed and validated to assess neurogenic bowel dysfunction in MS. All articles published until April 2020 were included. The following keywords were used: "neurogenic bowel dysfunction", "constipation", "fecal incontinence", "anorectal disorders", "multiple sclerosis".
In addition a single trained nurse performed qualitative interviews with patients suffering from ano rectal disorders secondary to MS. These interviews were lead in two phases. First part allowed to determine the wording of the different symptoms and mode of response for each item. The second part of the face-to-face was free and patients could express themselves if there was a gap in our list of symptoms.
During this first phase of the study a panel of 8 experts was selected, composed of neuro urologists and gastro enterologists.
The first version of the questionnaire was made based on the patients' qualitative interviews, on the reactions and comments of the expert team and on the literature review.
Step 2: Feasibility study The feasibility study was conducted between April 2020 and June 2020. This pilot study included 30 patients and was performed to assess comprehension, acceptability and pertinence of the items the investigators have created to build the questionnaire. More of response was also evaluate by patients.
Step 3: Validation study. This part of the study was performed between June2020 and April 2021. Validation study allowed to determine the psychometric properties of the new tool. All items were discussed for ceil or floor effect by the expert team. Each item with more than 50% of patients having the same response were discussed by panel experts to decide if they were excluded or not of the final version.
To obtain good psychometric properties, the investigators included 10 patients for each items of the questionnaire in the final version. This number of subjects was calculated to allow univariate and multivariate logistic regression.
Internal consistency reliability was calculated using the alpha coefficient of Cronbach. Each response has been transformed in a numeric value to perform this test. Alpha coefficient of Cronbach was considered as very good if > 0.7.
Test-retest reliability was tested using the intraclass correlation coefficient (ICC) which was significant over 0.7. The first questionnaire was filled at the end of the first consultation and patients had to mail a second questionnaire (filled at home) 7 to 14 days after the first consultation.
Statistical analyses: Final version of STAR-Q (Symptoms and Treatment Assessment of Ano-Rectal disorders in multiple sclerosis patients Questionnaire) was composed by 3 sub domains. First one was symptoms, second one was treatment, and a third sub domain was quality of life.
For each sub domains, the investigators calculated an alpha coefficient of Cronbach and a ICC. the investigators also assessed these properties for total score.
Total score was compared to NBD total score which represents gold standard in ano rectal disorders and thus constitutes the reference testing external consistency. Finally, PGI (Patient Global Improvment) severity scores were used to determine category of severity for STAR-Q scores.
All statistical analyzes were performed with the R-studio version 3.3.1 and Statviews (SAS institute V 5.0).
- Conditions
- Multiple Sclerosis, Constipation, Fecal Incontinence
- Being tested
- Clinical interviews
- Keywords
- multiple sclerosis, constipation, fecal incontinence, questionnaire, evaluation, quality of life
- Medical subject headings
- Multiple Sclerosis, Constipation, Fecal Incontinence
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Clinical interviewsOther
Also called Semi-qualitative interviews and questionnaire
Semi-qualitative interviews and questionnaire STAR-Q
| Study group | Role | What they receive |
|---|---|---|
| Patients enrolled | Patients with Multiple sclerosis, with an age older than 18 years old and symptoms of fecal incontinence or chronic constipation Receives: Other: Clinical interviews |
What is being measured
The primary outcome is the main question the study is designed to answer.
Reproductibility of STAR-Q
Patients were asked to answer a second time the questionnaire with a second evaluation at 14 days after the first one. The "intra-class correlation coefficient" (ICC) was used to determine if these evaluations could lead to similar results for each question. An ICC > 0.70 was necessary to define reproducibility.
Measured: 1 day
Acceptability and comprehension of STAR-Q
Each patient was asked to rate each version of the 22 questions with a four-point Likert scale (A: perfect, B: good, C: average, D: bad) regarding acceptance and comprehension of the questions.
Measured: 1 day
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted9 Aug 2021
- Study start1 Jun 2019
- Primary completion1 Jul 2020
- Study completion30 Apr 2021
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Multiple SclerosisStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 200 participants (actual)
Sponsor and investigators
- Lead sponsor
- Pierre and Marie Curie University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Gérard Amarenco, Pierre and Marie Curie University
- Investigators
- Gérard Amarenco, PHD, Principal investigator, Sorbonne Université, GRC 001, GREEN, AP-HP, Hôpital Tenon, F-75020, Paris, France
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04996186
- Sponsor's protocol ID
- GRC 01 GREEN STAR Q
- Acronym
- STAR-Q
- Status last verified
- Aug 2021
- First submitted
- 30 Jul 2021
- Last updated
- 27 Aug 2021
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided
Study at a glance
From the registry record, last updated by the sponsor on 27 Aug 2021. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Symptoms and Treatment Assessment of Ano-Rectal Disorders in Multiple Sclerosis Patients : STAR-Q (STAR Questionnaire): Validation of a New Tool to Better Explore and Manage Bowel Dysfunction.
- ClinicalTrials.gov ID
- NCT04996186
- Acronym / sponsor ID
- STAR-Q / GRC 01 GREEN STAR Q
- Conditions
- Multiple Sclerosis, Constipation, Fecal Incontinence
- Keywords
- multiple sclerosis, constipation, fecal incontinence, questionnaire, evaluation, quality of life
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 200 participants (actual)
- Lead sponsor
- Pierre and Marie Curie UniversityUniversity, hospital or other
- Study start
- 1 Jun 2019 (actual)
- Primary completion
- 1 Jul 2020 (actual)
- Study completion
- 30 Apr 2021 (actual)
- First posted
- 9 Aug 2021 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Multiple sclerosis (MS) is known to cause urinary disorders, sexual and bowel dysfunction. Urinary symptoms due to MS are well known and profit of multiple questionnaire or tool developed in MS patients.
Prevalence of bowel disorders in MS is difficult to assess. Some studies up to 70% bowel disorders in MS patients. Constipation and fecal incontinence are the two main symptoms in neurogenic bowel dysfunction and frequently coexist in this population, generally in association with urinary disorders.
Because of the high prevalence of bowel disorders their and the major impact on the quality of life of patients with Multiple sclerosis (PwMS) , and the cross-talk bladder-rectum (persistence of anorectal dysfunction leading to poor neurogenic bladder control) assessment of bowel disorders in MS is necessary. But this evaluation is difficult as no specific score exist. The neurogenic Bowel Dysfunction score (NBD) is often used. The NBD was developed and validated for spinal cord injury (SCI) population but not for PwMS MS. Yet NBD is often used in research for all neurologic patients despite its lack of sensibility in various neurogenic population other than spinal cord injury patient. As recommended in a Cochrane revue in 2014, there is a need of a specific evaluation for bowel symptoms in neurogenic population, especially for PwMS.
The aim of the study was to create and validate a new multidimensional questionnaire to assess bowel dysfunction and impact on quality of life in patients with MS.
The investigators conducted a prospective multicenter study (8 centers) between June 2019 to April 2021. This study was developed in 3 steps. First step was literature review and qualitative interview. Then the second step was the feasibility study to evaluate comprehension, acceptability of the different items. The last part of the study was the validation study of the questionnaire. This part of the study was performed between June2020 and April 2021. Validation study allowed to determine the psychometric properties of the new tool.
Patients aged over 18 years with multiple sclerosis diagnosed on the 2017 revised McDonald's criteria were included. Patients not able to read or understand the objectives and procedures for conducting the protocol and patient who had a recent relapse of MS were excluded.
Detailed description
Multiple sclerosis (MS) is an autoimmune autoimmune central nervous system (CNS) disorder characterized by demyelinisation and central neurologic damage. MS is the first cause of disability in young adults and affects 2.8 million people in the world.
Multiple sclerosis (MS) is known to cause urinary disorders, sexual and bowel dysfunction. Urinary symptoms due to MS are well known and profit of multiple questionnaire or tool developed in MS patients.
Prevalence of bowel disorders in MS is difficult to assess. Some studies up to 70% bowel disorders in MS patients. Constipation and fecal incontinence are the two main symptoms in neurogenic bowel dysfunction and frequently coexist in this population, generally in association with urinary disorders. Chronic constipation and fecal incontinence were defined by Rome IV criteria. According to these criteria, constipation is a bowel disorder in which symptoms of difficult, infrequent, or incomplete defecation predominate for at least 3 months and fecal incontinence is defined as the recurrent uncontrolled passage of fecal material for at least 3 months.
Moreover, neurogenic bowel dysfunction has a real impact on quality of life and can cause social isolation.
Because of the high prevalence of bowel disorders their and the major impact on the quality of life of patients with Multiple sclerosis (PwMS) , and the cross-talk bladder-rectum (persistence of anorectal dysfunction leading to poor neurogenic bladder control) assessment of bowel disorders in MS is necessary. But this evaluation is difficult as no specific score exist. The neurogenic Bowel Dysfunction score (NBD) is often used. The NBD was developed and validated for spinal cord injury (SCI) population but not for PwMS MS. Yet NBD is often used in research for all neurologic patients despite its lack of sensibility in various neurogenic population other than spinal cord injury patient. As recommended in a Cochrane revue in 2014, there is a need of a specific evaluation for bowel symptoms in neurogenic population, especially for PwMS.
The aim of the study was to create and validate a new multidimensional questionnaire to assess bowel dysfunction and impact on quality of life in patients with MS.
The investigators conducted a prospective multicenter study (8 centers) between June 2019 to April 2021. This study was developed in 3 steps. First step was literature review and qualitative interview. Then the second step was the feasibility study to evaluate comprehension, acceptability of the different items. The last part of the study was the validation study of the questionnaire. All these phases allowed a full psychometric validation of the questionnaire.
Patients aged over 18 years with multiple sclerosis diagnosed on the 2017 revised McDonald's criteria were included. Patients not able to read or understand the objectives and procedures for conducting the protocol and patient who had a recent relapse of MS were excluded.
Step 1: literature review and qualitative interview. The investigators conducted a review of literature on Pubmed to know all the existing questionnaires or tools developed and validated to assess neurogenic bowel dysfunction in MS. All articles published until April 2020 were included. The following keywords were used: "neurogenic bowel dysfunction", "constipation", "fecal incontinence", "anorectal disorders", "multiple sclerosis".
In addition a single trained nurse performed qualitative interviews with patients suffering from ano rectal disorders secondary to MS. These interviews were lead in two phases. First part allowed to determine the wording of the different symptoms and mode of response for each item. The second part of the face-to-face was free and patients could express themselves if there was a gap in our list of symptoms.
During this first phase of the study a panel of 8 experts was selected, composed of neuro urologists and gastro enterologists.
The first version of the questionnaire was made based on the patients' qualitative interviews, on the reactions and comments of the expert team and on the literature review.
Step 2: Feasibility study The feasibility study was conducted between April 2020 and June 2020. This pilot study included 30 patients and was performed to assess comprehension, acceptability and pertinence of the items the investigators have created to build the questionnaire. More of response was also evaluate by patients.
Step 3: Validation study. This part of the study was performed between June2020 and April 2021. Validation study allowed to determine the psychometric properties of the new tool. All items were discussed for ceil or floor effect by the expert team. Each item with more than 50% of patients having the same response were discussed by panel experts to decide if they were excluded or not of the final version.
To obtain good psychometric properties, the investigators included 10 patients for each items of the questionnaire in the final version. This number of subjects was calculated to allow univariate and multivariate logistic regression.
Internal consistency reliability was calculated using the alpha coefficient of Cronbach. Each response has been transformed in a numeric value to perform this test. Alpha coefficient of Cronbach was considered as very good if > 0.7.
Test-retest reliability was tested using the intraclass correlation coefficient (ICC) which was significant over 0.7. The first questionnaire was filled at the end of the first consultation and patients had to mail a second questionnaire (filled at home) 7 to 14 days after the first consultation.
Statistical analyses: Final version of STAR-Q (Symptoms and Treatment Assessment of Ano-Rectal disorders in multiple sclerosis patients Questionnaire) was composed by 3 sub domains. First one was symptoms, second one was treatment, and a third sub domain was quality of life.
For each sub domains, the investigators calculated an alpha coefficient of Cronbach and a ICC. the investigators also assessed these properties for total score.
Total score was compared to NBD total score which represents gold standard in ano rectal disorders and thus constitutes the reference testing external consistency. Finally, PGI (Patient Global Improvment) severity scores were used to determine category of severity for STAR-Q scores.
All statistical analyzes were performed with the R-studio version 3.3.1 and Statviews (SAS institute V 5.0).
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Patients enrolled | – | Other: Clinical interviewsPatients with Multiple sclerosis, with an age older than 18 years old and symptoms of fecal incontinence or chronic constipation |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- Patients consulting or hospitalized in a rehabilitation center or in a neuro-urology center
Key inclusion criteria (2 listed)
- Patients with multiple sclerosis diagnosed on the 2017 revised McDonald's criteria
- over 18 years old
Key exclusion criteria (2 listed)
- inability to read and to understand the questions
- recent relapse of multiple sclerosis
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Clinical interviewsAlso: Semi-qualitative interviews and questionnaireSemi-qualitative interviews and questionnaire STAR-Q | Other | Patients enrolled |
Primary outcome
Reproductibility of STAR-Q
Time frame: 1 day
Patients were asked to answer a second time the questionnaire with a second evaluation at 14 days after the first one. The "intra-class correlation coefficient" (ICC) was used to determine if these evaluations could lead to similar results for each question. An ICC > 0.70 was necessary to define reproducibility.
Acceptability and comprehension of STAR-Q
Time frame: 1 day
Each patient was asked to rate each version of the 22 questions with a four-point Likert scale (A: perfect, B: good, C: average, D: bad) regarding acceptance and comprehension of the questions.
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 27 Aug 2021.
- Individual participant dataSharing planned: Undecided
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Gérard Amarenco, PHD principal investigator
Sorbonne Université, GRC 001, GREEN, AP-HP, Hôpital Tenon, F-75020, Paris, France
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Multiple Sclerosis and Constipation, run by Pierre and Marie Curie University at 1 site in France.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 2 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 27 Aug 2021. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in France. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Reproductibility of STAR-Q (time frame: 1 day). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 27 Aug 2021.