SPOtMom: Survey on Patients After Childbearth Following Bariatric Surgery

Sponsor
Wuerzburg University Hospital (Other)
Overall Status
Recruiting
CT.gov ID
NCT04297956
Collaborator
(none)
70
5
35.9
14
0.4

Study Details

Study Description

Brief Summary

Women with a history of bariatric surgery may face various difficulties during pregnancy and puerperal time. Therefore it is assumed the prevalence of mental health disorders might be higher than in average women during and after pregnancy. This could possibly lead to an unsatisfying weight progress and therapeutic non-adherence. These factors shall be observed in the study in order to characterize this special cohort of participants.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Women following bariatric surgery are included at least 6 months after childbirth to evaluate retrospectively pregnancy and puerperal time. For mental health issues questionnaires, a structured clinical interview (SCID) and a psychological interview give an insight to past and present status. In order to evaluate weight progress and nutrient deficiencies routine follow-up care data of bariatric surgery is screened. In order to assess the course of pregnancy and child development data is extracted from pregnancy and child's examinations reports. Furthermore medication adherence, quality of life and sleep are registered by questionnaires.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    70 participants
    Observational Model:
    Cohort
    Time Perspective:
    Retrospective
    Official Title:
    Survey on Patients After Childbearth Following Bariatric Surgery - Data Collection on Mental Health Complications, Weight Change, Nutrition Deficiencies and Postpartal Progress
    Actual Study Start Date :
    Feb 5, 2020
    Anticipated Primary Completion Date :
    Feb 1, 2023
    Anticipated Study Completion Date :
    Feb 1, 2023

    Outcome Measures

    Primary Outcome Measures

    1. Number of patients with prevalence of symptoms of depression or anxiety assessed by questionnaires and structured clinical interview (SCID) [date of recruitement (> 6 months after childbirth)]

      questionnaires for depression: Beck Depression Inventory (BDI-II) Patient Health Questionnaire-9 (PHQ-9) Edinburgh Postnatal Depression Scale (EPDS) questionnaire for anxiety: Generalized Anxiety Disorder-7 (GAD-7) Prevalence of symptoms can be defined by scores higher than defined cut-offs in questionnaires or scores that lead to diagnosis of psychiatric disorder in structured clinical interview

    2. Number of patients with prevalence of symptoms of depression or anxiety assessed by questionnaires and structured clinical interview [retrospective: time frame 0-4 weeks after birth]

      questionnaires for depression: Patient Health Questionnaire-9 (PHQ-9) questionnaire for anxiety: Generalized Anxiety Disorder-7 (GAD-7) Prevalence of symptoms can be defined by scores higher than defined cut-offs in questionnaires or scores that lead to diagnosis of psychiatric disorder in structured clinical interview

    3. Number of patients with prevalence of symptoms of depression assessed by structured clinical interview [retrospective: complete lifetime from date of birth until date of recruitment (> 6 months after childbirth), assessed up to 50 years]

      Prevalence of symptoms can be defined by scores that lead to diagnosis of psychiatric disorder in structured clinical interview

    Secondary Outcome Measures

    1. Mean change of body weight from baseline [from date of bariatric surgery until date of recruitment (> 6 months after childbirth), assessed up to 20 years]

      Body weight is measured on scales and participants are asked additionally via questionnaire. Baseline measurement starts at date of bariatric surgery.

    2. Status of nutritional deficiencies and therapy adherence [from date of bariatric surgery until date of recruitment (> 6 months after childbirth), assessed up to 20 years]

      Participants are asked to answer Medication Adherence Report Scale (MARS-D) and blood levels concerning nutrients that are examined routinely in bariatric surgery follow-up care are analysed.

    3. Adverse events in pregnancy and child development [from date of beginning of pregnancy until date of recruitment (> 6 months after childbirth), assessed up to 12 years]

      Record of prenatal care and record of child's examinations are screened for complications.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    Female
    Inclusion Criteria:
    • 18 years of age

    • status following bariatric / metabolic surgery due to indication criteria

    • childbirth after bariatric / metabolic surgery, at least 6 months ago

    • written informed consent

    Exclusion Criteria:

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 University Hospital Würzburg Bavaria Germany 97080
    2 Sana Adipositaszentrum Offenbach Offenbach am Main Hessen Germany 63069
    3 Uniklinikum Aachen, Klinik für Allgemein-, Viszeral-und Transplantationschirurgie Aachen Nordrhein-Westfalen Germany 52074
    4 Sana Adipositaszentrum NRW Remscheid Nordrhein-Westfalen Germany 42853
    5 Adipositaszentrum Westküstenklinium Heide Heide Schleswig-Holstein Germany 25746

    Sponsors and Collaborators

    • Wuerzburg University Hospital

    Investigators

    • Principal Investigator: Ann-Cathrin Koschker, Dr. med., Würzburg University Hospital

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Ann-Cathrin Koschker, Head of outpatient clinic for diabetes and lipids, Wuerzburg University Hospital
    ClinicalTrials.gov Identifier:
    NCT04297956
    Other Study ID Numbers:
    • spot_mom
    First Posted:
    Mar 6, 2020
    Last Update Posted:
    Feb 1, 2022
    Last Verified:
    Jan 1, 2022
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Feb 1, 2022