About this trial
Introduction. Distasis rectus abdominis (DRA) is defined as the presence of divergence between the rectus abdominis muscles along the linea alba. Some authors describe a prevalence of 40% in women up to one year postpartum. Some studies suggest that the presence of DRA can be related to the appearance of low back, pelvic and abdominal pain and even urinary incontinence. These factors can significantly affect the quality of life of women with diastasis both socially, sexual and personal level. According to several studies, this pathology is related to higher rates of depression and an alteration in the self-perception of body image that makes these women to look to specialized medical care.
At present, the quantitative evaluation of DRA is performed purely anatomically. This evaluation consists in measuring the separation between the two rectus abdominis. Currently there is no consensus as to the protocol that should be used for this measurement.
So far, no instrument is able to quantitatively measure the consequences of DRA. The evaluation of symptoms and consequences should include relevant parameters such as quality of life, perception of body image and functional limitations.
The objective of this study is the creation and validation of a specific questionnaire to evaluate the symptoms and consequences of DRA.
Material and methods. A) Development of the questionnaire
1. Literature review 2. Online survey 3. Expert panel 4. Pilot test of the questionnaire
B) Validation of the questionnaire. The psychometric properties of the questionnaire will be evaluated in a sample of patients with DRA. The sample will be composed of a group of adult women with DRA who attended to a physiotherapy clinic.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
subjects with diastasis recti,
adult,
women.
Disqualifiers
cognitive disabilities that can difficult a good understanding of the questionnaire,
lack of knowledge of Spanish language.
ventral hernia.
previous abdominal surgeries.
Trial population
Adult women with diastasis recti attending to a physiotherapist or midwive center will be proposed to participate in the study. A signed informed consent will be necessary to participate in this research.
Trial design
Other
Prospective
Treatments tested in this trial
Questionnaire
Diagnostic testA battery of questionnaires will be propose to the participants
Treatment groups
Trial outcomes
Primary outcomes
Diastasis abdominal consequences
Diastasis rectus abdominis consequences will be measured using the Diastasis rectus abdominis questionnaire
Secondary outcomes
Inter-recti distance
The distance between the two medial borders of rectus abdominis muscles will be measured using ultrasound
Subjective well-being
Subjective well-being will be measured using the World Health Organization Quality-of-Life Scale (WHOQOL-Bref) "overall quality of life and general health" subscale (2-10 points). Domain scores are scaled in a positive direction, higher scores denote higher quality of life.
Gastrointestinal symptoms
Gastrointestinal symptoms will be measured using the Gastrointestinal Quality of Life Index (GIQLI) "Symptoms" subscale (0-36 points). 4-likert scale ( 0 points being the worst punctuation and 4 points the best)
Functioning
Functioning will be measured using the World Health Organization Disability Assessment Schedule-36 (WHODAS-36) "mobility" and "life activities"subscales (0-36points). 5- point Likert scale. Higher scores indicate lower quality of life.
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
University of Valencia
Lead sponsor
University Hospital, Caen
Collaborator