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Body Image clinical trials

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NCT ID: NCT04993235 Recruiting - Body Image Clinical Trials

Body Perception and Representation in Overgrowth Syndromes, Behavioral Assessment and Neuropsychological Development

Body-PROBAND
Start date: May 28, 2021
Phase:
Study type: Observational

Sotos Syndrome (SS) and Beckwith-Wiedemann Syndrome (BWS) are known as overgrowth syndromes as they involve an excessive growth of the whole body or of specific body parts. Beyond their primary physical problems, people with SS and BWS could present cognitive delay, socio-emotional and social behavior difficulties. For the SS, previous research reported impairments in specific neuropsychological domains and alterations of social behavior. Nevertheless, a description of the neuropsychological and behavioral profile in developmental age is still lacking. For the BWS, only in recent years alterations in social-cognitive development and in social behavior have started to gain attention of clinicians and researchers. However, no study has investigated the neuropsychological and behavioral functioning of children and adolescents with BWS. In this light, this research project aims at providing the first detailed description of the neuropsychological and behavioral profile of children and adolescents with SS and BWS. Moreover, patients with SS and BWS experience structural alterations of their bodies and are early exposed to invasive diagnostical and medical procedures, which could interfere with the development of body representation. Body representation starts forming early in life through the integration of exteroceptive and interoceptive information, and plays a pivotal role in the social-cognitive development. Given the changes occurring in puberty and the crucial importance of body image in the relationship with peers, adolescence could be seen as a critical period for studying body representation. Thus, this project would investigate body representation at multiple levels (i.e. body image, body schema and interoceptive perception) and evaluate their impact on social-cognitive abilities in adolescents with SS and BWS. It is expected that both the clinical groups show alterations of body representation compared to healthy peers, and that these alterations could associate with impairments in affect recognition and regulation.

NCT ID: NCT04677400 Recruiting - Body Image Clinical Trials

More Than Body Appearance (MBA) Intervention

Start date: November 16, 2020
Phase: N/A
Study type: Interventional

The link between sport, physical exercise, and body image depends on the reasons underlying an individual's desire to engage in sport and physical exercise. Individuals characterized by reasons for exercise related to physical appearance are likely to focus on factors such as the number of calories burned, reductions in body weight, or visible changes in physical appearance during the practice; in accordance, appearance-related reasons for exercise are associated with body dissatisfaction and disordered eating. In contrast, reasons to exercise unrelated to physical appearance (such as health and enjoyment) are associated with body satisfaction. Thus, only certain reasons for exercise are associated with positive body image outcomes. Recently, literature studies affirmed that experimental designs could manipulate the emphasis placed on function (as opposed to physical appearance) during sport practice and physical exercise to promote positive body image. Based on this evidence, the first objective of the study will be testing the effectiveness of a psychological online intervention (More than Body Appearance [MBA] intervention) targeting body image in improving body image in individuals practicing physical activity.

NCT ID: NCT03905070 Recruiting - Bariatric Surgery Clinical Trials

Investigation of Body Awareness and Affecting Factors in Bariatric Surgery Patients

Start date: March 1, 2019
Phase:
Study type: Observational

The aim of this study is to investigate the body awareness and the factors affecting the bariatric surgery.

NCT ID: NCT03637920 Recruiting - Body Image Clinical Trials

Sexuality in Transmen During Hormone and Operative Treatment

Transmann
Start date: July 30, 2018
Phase:
Study type: Observational

With this analysis the investigators aim at discovering a difference in sexuality between transmen, cissexual women and cissexual men. A potential impact of body satisfaction will also be explored. Furthermore the investigators want to assess the gender dysphoria in transmen.

NCT ID: NCT03591393 Recruiting - Pregnancy Related Clinical Trials

Pelvic Floor Dysfunction and Its Influence on Body Image and Sexual Function

PFD-BI
Start date: August 1, 2018
Phase: N/A
Study type: Interventional

The first objective to determinate the prevalence of pelvic floor dysfunction in pregnant women and in the first year postpartum. The second objective is to assess the anatomical (both clinical and ultrasound), demographic and obstetric variables in symptomatic women and their association with pelvic floor dysfunction, sexual function and Body Image. This is a single center prospective cohort study. Women will be asked to fill out a questionnaire at the time of their 1st and 3rd trimester scan, at the postpartum checkup and 12 months postpartum. Furthermore, they will undergo a pelvic floor ultrasound at the time of their first and third trimester scan. The presence of pelvic floor dysfunctions will be recorded through validated self-administered questionnaires with five domains: Wexner questionnaire for anal incontinence, PAC-SYM for constipation, International Consultation on Incontinence Questionnaire Short Form for urinary incontinence, the Pelvic Organ Prolapse Distress Inventory for pelvic organ prolapse, POP/UI Sexual Questionnaire - IUGA revised for sexual function. The body image perception will be assessed using the Dutch-validated version of the self-administered Body Image Disturbance Questionnaire. The anatomy of the pelvic floor will be objectively assessed off line on 3D/4D transperineal ultrasound volumes and POP-Q examination. The demographic variables and information about the pregnancy and the delivery will be obtained from the medical records.

NCT ID: NCT00625053 Recruiting - Quality of Life Clinical Trials

Functional Outcome After Incisional Hernia Repair: Open Versus Laparoscopic Repair

GINCISHERNIA
Start date: April 2008
Phase: Phase 4
Study type: Interventional

Background: Midline incisional hernia is reported from 0,5 to 11% after abdominal operations. Primary repair without mesh reinforcement is almost abandoned because of high recurrence rates (24 to 46%). Use of prosthetic mesh in incisional hernia repair lowered the recurrence rates under 10%. Recurrence rate alone is not the main quality criterion for incisional hernia repair anymore. Large series and meta-analyses confirmed the value of laparoscopic repair as at least equal if not better compared with open repair. Discomfort, pain, diminished quality of life and body image alteration influences functional well being. No baseline information exists in any of these fields treating pre- or post-operative phases in patients with incisional hernia. Respiratory functions and medico-economic evaluation are other rarely investigated fields that we consider in our trial. The objective of this study is to analyse the functional outcome status of patients after laparoscopic incisional hernia repair compared to open repair. Methods: A randomized controlled non-blinded clinical trial is designed to compare laparoscopic incisional hernia mesh repair with open repair on post operative pain, health related quality of life outcomes, body image and cosmetic measurements, respiratory functions, recurrence rates, and cost. Volunteers will be recruited in Geneva University Hospital, department of surgery, visceral surgery unit. Eligibility criteria is male patient aged over 18 years, with reducible incisional hernia who are candidates for elective surgery and medically fit for general anesthesia.30 patients will be enrolled for each group. Follow-up will take place at 10th, 30th days as well as 3 12 and 24 post operative months by questionnaires and by clinical exam by independent expert. An overall cost-analysis will be realized. Patient enrollment in the study will start in April 2008 and estimated to end in september 2009.