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Completed

NCT Number: NCT00677508

Development of an Instrument to Measure Quality of Life in Children With Chronic Constipation and Soiling

We propose to develop parent and child disease-specific instruments to assess health related quality of life (HRQoL) in children with constipation and fecal incontinence.

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Key information

Age range

2 year–18 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Medical College of Wisconsin

Milwaukee, Wisconsin, 53226, United States

About this study

Chronic constipation is a common problem in childhood, accounting for almost 3% of consultations in pediatric practice. In many children constipation is accompanied by overflow soiling (fecal incontinence). This condition often gives rise to behavioral, social, and emotional problems.

We plan to develop a disease-specific instrument to assess HRQoL in children with constipation and fecal incontinence. We hypothesize that HRQoL is worse in children with fecal incontinence compared to children with constipation but no fecal incontinence. The instrument will involve both parent and child self-reporting measures and will enable researchers to evaluate how disease and treatment strategies impact both child and parent perceptions of quality of life. In the long run this will enable physicians to develop a child friendly approach to management of chronic constipation and fecal incontinence.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age 2-18 years
  • Child and parents fluent in English
  • Child must meet one of the following criteria;

A. Constipation and fecal incontinence: must include 2 or more of the following in a child with insufficient criteria for a diagnosis of IBS (criteria fulfilled at least once per week for at least 2 months before diagnosis in a child over 4 years of age and for at least one month in a child less than 4 years of age):

  • Two or fewer defecations in the toilet per week
  • At least 1 episode of fecal incontinence per week
  • History of retentive posturing or excessive volitional stool retention
  • History of painful or hard bowel movements
  • Presence of a large fecal mass in the rectum
  • History of large diameter stools that may obstruct the toilet

B. Constipation predominant IBS: must include the following, once a week for at least 2 months:

  • Abdominal pain/discomfort, associated with 2 of the following:
  • improved with defecation
  • onset associated with 2 or less stools per week
  • onset associated with hard or lump stool
  • no evidence of inflammatory, anatomic, metabolic or neoplastic processes.

C. Non retentive fecal incontinence: must include all of the following in a child with a developmental age of at least 4 years (criteria fulfilled at least once per week for at least 2 months before diagnosis) [4]:

  • Defecation into places inappropriate to the social context at least once per month.
  • No evidence of an inflammatory, anatomic, metabolic, or neoplastic process that explains the subject's symptoms
  • No evidence of fecal retention.

Exclusion criteria

  • Children with developmental delays and children over 12 years of age who are unable to understand the questionnaires.
  • Associated chronic disease which may have an impact on quality of life such as cerebral palsy, spine deformity or malformations, learning difficulties, severe mental illness, celiac disease, etc.
  • Child and parents not fluent in English.

Treatment and study plan

Primary outcomes

  1. To develop and validate child and parent questionnaires to assess HRQoL of children with chronic constipation and fecal incontinence.

    Time frame: 2 years

Sponsors and collaborators

Lead sponsor

Medical College of Wisconsin

Other

Collaborators

  • Boston Children's Hospital
  • Ohio State University
  • Takeda Pharmaceuticals North America, Inc.
  • University of South Alabama
  • University of Texas Southwestern Medical Center

Registry information

Important dates

Study start
2005
Primary completion
2011
Study completion
2011
First posted
May 14, 2008
Registry last updated
Apr 30, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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