SAPPH
Paris, 75014, France
NCT Number: NCT02727010
Background Women with rare diseases resulting in motor disabilities wishing to become mother face a major challenge. The investigators hypothesize that provided with adequate support, they are able to achieve a successful pregnancy and to offer their child a safe family environment.
Methods To test this hypothesis, the investigators shall conduct a prospective observational prospective survey of a consecutive series of volunteer pregnant women or mothers of children less than 14 months, with motor impairment, participating in a program of parenting support developed in our institution.
Primary outcome: social environment, child development, mother-infant attachment, mother- infant interactions Secondary outcome: social and demographic characteristics, severity of motor impairment, associated impairment, perinatal morbidity for the mother and the infant (composite indicator), emotional status, and the needs expressed by women regarding the level of medical or social care.
Analysis The investigators shall describe the distribution of the primary outcome measurements in the subgroup of women with motor impairment related to a rare disease. The investigators shall compare this distribution to the expected distribution in the general population, and to that observed in women with motor impairment unrelated to a rare disease. The investigators shall also study primary outcome measurements as a function of the severity of maternal disability, of the mother's social characteristics and emotional status.
The investigators shall also describe the distribution the distribution of perinatal morbidity globally, and as a function of the potential explanatory variables mentioned above.
The investigators shall also report on the opinion of women regarding the support they were offered so far, and the support they declare they should benefit from.
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Notify Me18 year and older
Female
Observational
Paris, 75014, France
Background Women with motor disabilities have the same well-founded desire to become a mother as other women. Despite dedicated aids and adapted supportive measures, they face social blame from persons who believe they are not apt to provide adequate care to their children. When a rare disease caused the disability, planning to become a mother is even more critical, since most perinatal care providers are unfamiliar with the condition, and specialists of the disease are unfamiliar with pregnancy. Unsurprisingly, data on motherhood in women with rare diseases resulting in motor impairment are scarce.
The institutions of the investigators run a joint care program dedicated to future parents and parents with disabilities, namely:
The investigators felt the need to evaluate the outcome of our program, in terms of quality of infant environment, development, attachment, and interactions with their disabled mother. The investigators focused on parenthood in women with a rare disease resulting in motor impairment, a research field remaining largely unexplored so far.
Hypothesis Our hypothesis is that when provided with a specific care program, mothers with motor impairment due to a rare disease and their partners have the capacity to offer their children appropriate social environment and care, resulting in child development, mother-infant attachment, and mother- infant interactions being similar to what one would expect in women without motor impairment.
Objective Primary objective To describe social environment, child development, mother-infant attachment, mother- infant interactions, when the mother has motor impairment due du a rare disease.
Secondary objective
Eligibility criteria Please see specific box
Outcome measurements (assessed at least once before the age of 14 months, see specific box) Primary outcome Child development /Infant attachment /Social environment /Mother infant interaction/ Child protection legal decisions if applicable Secondary outcome Demographic and social characteristics Disease or event causing impairment Obstetrical history Somatic and psychic events before, during pregnancy, and post-partum History of access to care Severity of impairment and handicap Maternal emotional status Needs expressed by women regarding medical care, psychological, social, and environmental support
Study design Pre inclusion: written and verbal information on the study to all women with motor impairment seeking care either at the Pitié Salpétrière Maternity unit or at the Service d'Aide à la Parentalité pour les Personnes en Situation de Handicap (SAPPH) Inclusion visit: During a planned training session, either pre natal or post natal Follow up visit: once of twice before the child is 14 months. A specific consent of both parents will be required for all outcome criteria concerning the infant.
Research visits will take place during usual visits of our parenthood support and training program.
Analysis The investigators shall describe the distribution of the primary outcome measurements in the subgroup of women with motor impairment related to a rare disease. The investigators shall compare this distribution to the expected distribution in the general population, and to that observed in women with motor impairment unrelated to a rare disease. The investigators shall also study primary outcome measurements as a function of the severity of maternal disability, of the mother's social characteristics and emotional status.
The investigators shall also describe the distribution the distribution of perinatal morbidity globally, and as a function of the potential explanatory variables mentioned above.
the investigators shall also report on the opinion of women regarding the support they were offered so far, and the support they declare they should benefit from.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: At least once before the age of 14 months. May be repeated twice.
Child development assessed by Brunet Lézine score: based on standardized examination of the infant by a trained child psychologist
Time frame: At least once before the age of 14 months. May be repeated twice.
Infant attachment assessed by Guedenet and Fermanian ADBB scale: scale assessed by investigator
Time frame: At least once before the age of 14 months. May be repeated twice.
Social environment assessed by Cutrona scale: self-administered questionnaire
Time frame: At least once before the age of 14 months. May be repeated twice.
assessed by:
Time frame: At lest once before the age of 14 months. May be repeated twice.
Demographic and social characteristics, qualitative variables (Questionnaire administered by investigator)
Time frame: At lest once before the age of 14 months. May be repeated twice.
Epices score of social deprivation (Self-administered questionnaire)
Time frame: At lest once before the age of 14 months. May be repeated twice.
Disease or event causing impairment: preset qualitative variables (Questionnaire administered by investigator)
Time frame: At lest once before the age of 14 months. May be repeated twice.
Obstetrical history: preset qualitative variables (Questionnaire administered by investigator)
Time frame: At lest once before the age of 14 months. May be repeated twice.
Time frame: At lest once before the age of 14 months. May be repeated twice.
History of access to care: standardized interview (Questionnaire administered by investigator)
Time frame: At lest once before the age of 14 months. May be repeated twice.
Barthel score of capacity in everyday life (Self-administered questionnaire)
Time frame: At lest once before the age of 14 months. May be repeated twice.
Time frame: At lest once before the age of 14 months. May be repeated twice.
Assessed by STAI / EPDS scales (Self-administered questionnaire)
Time frame: At lest once before the age of 14 months. May be repeated twice.
Assessed self-administered questionnaire
Assistance Publique - Hôpitaux de Paris
Other
Parenthood and Motherhood in Women With Motor Impairment and Disability Related to a Rare Disease
Acronym: MMOMA
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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