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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.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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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
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.

France1 site
  • Department of Neuro- Urology, Hôpital Tenon

    Paris, 75020

Other trials in France

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).

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 groups in NCT04996186
Study groupRoleWhat they receive
Patients enrolledPatients 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.

  1. 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

  2. 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.

  1. First posted9 Aug 2021
  2. Study start1 Jun 2019
  3. Primary completion1 Jul 2020
  4. Study completion30 Apr 2021

Resources

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)
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

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.

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