Disability EvaluationMMOMANCT02727010
Motherhood With MOtor Impairment Due to MAlady (Rare Disease)
An observational study of Disability Evaluation and Child of Impaired Parents, run by Assistance Publique - Hôpitaux de Paris at 1 site in France.
Trial summary
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. Read more about this study
- Who is it for?
- Ages 18 years and older, women only
- Conditions the study is for
- Disability Evaluation, Child of Impaired Parents
- How many people
- 29 participants
- Where
- 1 siteFrance
- Study dates
- 2 Mar 2016to 28 Nov 2017
- 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
- Women only
- No healthy volunteers
- Adult, Older adult
Study population: Pregnant women or mothers to children < 14 months, with motor impairment, visiting the inclusion center and willing to participate in the study. Any motor impairment available, regardless of its cause.
Who may be able to join
- Women aged 18 or older
- Either pregnant > 14 weeks, or mother of a child < 1 year
- With disability resulting from motor impairment
- Giving informed consent
- With social insurance
Who cannot join
- Know mental retardation
- Known psychiatric disorder
- Not fluent in French
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Parenthood and Motherhood in Women With Motor Impairment and Disability Related to a Rare Disease
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.
Read more
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.
Read the detailed description
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:
- Hôpital Universitaire Pitié Salpêtrière- Charles Foix (assistance Publique Hôpitaux de Paris and Université Paris 6), providing a gynecological and perinatal unit with care programs adapted to women with disabilities, plus a number of reference centers for rare neurologic and muscular diseases including research and clinical care.
- Service d'Aide à la Parentalité des Personnes en Situation de Handicap (SAPPH, Fondation Hospitalière Sainte Marie) providing training and support to parenthood to persons with motor or sensory disabilities. This training program aims at recognizing parental capacities, and if necessary enhancing them by information, training, adapting the environment, or seeking extra human help.
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
- To describe maternal and perinatal outcome when the mother has motor impairment due du a rare disease
- To explore a potential relation between the outcome criteria of the primary goal with
- The severity of motor impairment
- The causal disease
- The personal history of the mother including her access to adapted care prior to pregnancy during pregnancy and post-partum
- The social status of the family
- The emotional status of the mother
- To compare the distribution of primary goal outcome criteria in our study population to what is expected in the general population, when appropriate
- To compare the distribution of primary goal outcome criteria in our study population to what we observed in women with motor impairment that does not result from a rare disease
- To describe the needs expressed by women regarding medical care, psychological, social, and environmental support
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.
- Conditions
- Disability Evaluation, Child of Impaired Parents
- Keywords
- Motor disability, Motor impairment, Pregnancy, Parenthood, Child psychology
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
| Study group | Role | What they receive |
|---|---|---|
| mothers with motor impairment due to a rare disease | 20 Women with motor impairment due to a rare disease | |
| mothers with motor impairment not related to a rare disease | controls, 20 women with motor impairment not related to a rare disease |
What is being measured
The primary outcome is the main question the study is designed to answer.
Child development Mother infant attachment - Coding Interactive Behavior - Pirgas scale - Child protection legal decisions if applicable
Child development assessed by Brunet Lézine score: based on standardized examination of the infant by a trained child psychologist
Measured: At least once before the age of 14 months. May be repeated twice.
Infant attachment
Infant attachment assessed by Guedenet and Fermanian ADBB scale: scale assessed by investigator
Measured: At least once before the age of 14 months. May be repeated twice.
Social environment
Social environment assessed by Cutrona scale: self-administered questionnaire
Measured: At least once before the age of 14 months. May be repeated twice.
Mother infant interaction
assessed by:
- Coding Interactive Behavior: mother infant interaction filmed in a standardized fashion, and analyzed by trained psychologists blinded to the dyad's history.
- Pirgas scale: clinical diagnosis regarding mother to infant interactions Child protection legal decisions : type of decision if applicable.
Measured: At least once before the age of 14 months. May be repeated twice.
Secondary outcomes (10)
Demographic and social characteristics
Demographic and social characteristics, qualitative variables (Questionnaire administered by investigator)
Measured: At lest once before the age of 14 months. May be repeated twice.
Epices score of social deprivation
Epices score of social deprivation (Self-administered questionnaire)
Measured: At lest once before the age of 14 months. May be repeated twice.
Disease or event causing impairment
Disease or event causing impairment: preset qualitative variables (Questionnaire administered by investigator)
Measured: At lest once before the age of 14 months. May be repeated twice.
Obstetrical history
Obstetrical history: preset qualitative variables (Questionnaire administered by investigator)
Measured: At lest once before the age of 14 months. May be repeated twice.
Somatic and psychic events before, during pregnancy, and post-partum (composite scores)
Measured: At lest once before the age of 14 months. May be repeated twice.
History of access to care
History of access to care: standardized interview (Questionnaire administered by investigator)
Measured: At lest once before the age of 14 months. May be repeated twice.
Barthel score of capacity in everyday life
Barthel score of capacity in everyday life (Self-administered questionnaire)
Measured: At lest once before the age of 14 months. May be repeated twice.
Ad hoc ordinal score based on the number of body parts with motor impairment and additional non-motor impairment
Measured: At lest once before the age of 14 months. May be repeated twice.
Maternal emotional status
Assessed by STAI / EPDS scales (Self-administered questionnaire)
Measured: At lest once before the age of 14 months. May be repeated twice.
List of the needs expressed by women regarding medical care, psychological, social, and environmental support
Assessed self-administered questionnaire
Measured: At lest once before the age of 14 months. May be repeated twice.
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted4 Apr 2016 (estimated)
- Study start2 Mar 2016
- Primary completion28 Aug 2017
- Study completion28 Nov 2017
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Disability EvaluationStudies of the same condition, open and under way.
- More trials run by Assistance Publique - Hôpitaux de ParisThe sponsor's other registered studies.
- 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
- Case-control
- Time perspective
- Prospective
- Enrolment
- 29 participants (actual)
Sponsor and investigators
- Lead sponsor
- Assistance Publique - Hôpitaux de Paris
- Sponsor type
- University, hospital or other
- Collaborators
- Service d'Aide à la Parentalité des Personnes en Situation de Handicap (SAPPH)
- Responsible party
- Sponsor
- Investigators
- Drina Candilis, PhD, Principal investigator, SAPPH
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02727010
- Sponsor's protocol ID
- NI16003
- Acronym
- MMOMA
- Status last verified
- Dec 2016
- First submitted
- 29 Mar 2016
- Last updated
- 29 May 2018
- Results posted
- No
- Data monitoring committee
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 29 May 2018. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Parenthood and Motherhood in Women With Motor Impairment and Disability Related to a Rare Disease
- ClinicalTrials.gov ID
- NCT02727010
- Acronym / sponsor ID
- MMOMA / NI16003
- Conditions
- Disability Evaluation, Child of Impaired Parents
- Keywords
- Motor disability, Motor impairment, Pregnancy, Parenthood, Child psychology
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 29 participants (actual)
- Lead sponsor
- Assistance Publique - Hôpitaux de ParisUniversity, hospital or other
- Collaborators
- Service d'Aide à la Parentalité des Personnes en Situation de Handicap (SAPPH)
- Study start
- 2 Mar 2016 (actual)
- Primary completion
- 28 Aug 2017 (actual)
- Study completion
- 28 Nov 2017 (actual)
- First posted
- 4 Apr 2016 (estimated)
- 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.
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.
Detailed description
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:
- Hôpital Universitaire Pitié Salpêtrière- Charles Foix (assistance Publique Hôpitaux de Paris and Université Paris 6), providing a gynecological and perinatal unit with care programs adapted to women with disabilities, plus a number of reference centers for rare neurologic and muscular diseases including research and clinical care.
- Service d'Aide à la Parentalité des Personnes en Situation de Handicap (SAPPH, Fondation Hospitalière Sainte Marie) providing training and support to parenthood to persons with motor or sensory disabilities. This training program aims at recognizing parental capacities, and if necessary enhancing them by information, training, adapting the environment, or seeking extra human help.
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
- To describe maternal and perinatal outcome when the mother has motor impairment due du a rare disease
- To explore a potential relation between the outcome criteria of the primary goal with
- The severity of motor impairment
- The causal disease
- The personal history of the mother including her access to adapted care prior to pregnancy during pregnancy and post-partum
- The social status of the family
- The emotional status of the mother
- To compare the distribution of primary goal outcome criteria in our study population to what is expected in the general population, when appropriate
- To compare the distribution of primary goal outcome criteria in our study population to what we observed in women with motor impairment that does not result from a rare disease
- To describe the needs expressed by women regarding medical care, psychological, social, and environmental support
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.
Study design
- Observational model
- Case-control
- Time perspective
- Prospective
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| mothers with motor impairment due to a rare disease | – | –20 Women with motor impairment due to a rare disease |
| mothers with motor impairment not related to a rare disease | – | –controls, 20 women with motor impairment not related to a rare disease |
Who may qualify
- Ages
- 18 years and older
- Sex
- Female only
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- Pregnant women or mothers to children < 14 months, with motor impairment, visiting the inclusion center and willing to participate in the study. Any motor impairment available, regardless of its cause.
Key inclusion criteria (5 listed)
- Women aged 18 or older
- Either pregnant > 14 weeks, or mother of a child < 1 year
- With disability resulting from motor impairment
- Giving informed consent
- With social insurance
Key exclusion criteria (3 listed)
- Know mental retardation
- Known psychiatric disorder
- Not fluent in French
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Child development Mother infant attachment - Coding Interactive Behavior - Pirgas scale - Child protection legal decisions if applicable
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
Infant attachment
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
Social environment
Time frame: At least once before the age of 14 months. May be repeated twice.
Social environment assessed by Cutrona scale: self-administered questionnaire
Mother infant interaction
Time frame: At least once before the age of 14 months. May be repeated twice.
assessed by: * Coding Interactive Behavior: mother infant interaction filmed in a standardized fashion, and analyzed by trained psychologists blinded to the dyad's history. * Pirgas scale: clinical diagnosis regarding mother to infant interactions Child protection legal decisions : type of decision if applicable.
10 secondary outcomes
Demographic and social characteristics
Time frame: At lest once before the age of 14 months. May be repeated twice.
Epices score of social deprivation
Time frame: At lest once before the age of 14 months. May be repeated twice.
Disease or event causing impairment
Time frame: At lest once before the age of 14 months. May be repeated twice.
Obstetrical history
Time frame: At lest once before the age of 14 months. May be repeated twice.
Somatic and psychic events before, during pregnancy, and post-partum (composite scores)
Time frame: At lest once before the age of 14 months. May be repeated twice.
History of access to care
Time frame: At lest once before the age of 14 months. May be repeated twice.
Barthel score of capacity in everyday life
Time frame: At lest once before the age of 14 months. May be repeated twice.
Ad hoc ordinal score based on the number of body parts with motor impairment and additional non-motor impairment
Time frame: At lest once before the age of 14 months. May be repeated twice.
Maternal emotional status
Time frame: At lest once before the age of 14 months. May be repeated twice.
List of the needs expressed by women regarding medical care, psychological, social, and environmental support
Time frame: At lest once before the age of 14 months. May be repeated twice.
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 29 May 2018.
- Individual participant dataSharing planned: No
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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.
Drina Candilis, PhD principal investigator
SAPPH
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 Disability Evaluation and Child of Impaired Parents, run by Assistance Publique - Hôpitaux de Paris 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 5 inclusion and 3 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 29 May 2018. 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?
Child development Mother infant attachment - Coding Interactive Behavior - Pirgas scale - Child protection legal decisions if applicable (time frame: At least once before the age of 14 months. May be repeated twice.). The study lists 4 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 29 May 2018; AzTrials last refreshed its copy on 8 Nov 2026.