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Name: Marie-Eve Carrier

Email Address: carrier.marie.eve@gmail.com

Position: Research Associate  

Biography:

Marie-Eve Carrier is a Research Associate working with Dr. Brett Thombs since 2013. Marie-Eve graduated from the Université de Montréal in 2006, with a Master’s degree in Anthropology. Between 2006 and 2013, Marie-Eve coordinated many quantitative and qualitative studies in the perinatal mental health research field. Marie-Eve joined the SPIN team in March 2013. She coordinates SPIN’s projects and activities on a day-to-day basis. For the past years, she has been closely involved in the establishment and rapid growth of SPIN, which is composed of researchers, clinicians, and people living with scleroderma from around the world. Marie-Eve and the SPIN research team are working everyday towards fulfilling SPIN’s mission: providing people living with scleroderma free access to support programs to improve their quality of life.

Publications (selected):

Fox RS, Kwakkenbos L, Carrier ME, Mills SD, Gholizadeh S, Jewett LR, Roesch SC, Merz EL, Assassi S, Furst DE, Gottesman K, Mayes MD, Thombs BD, Marlcarne BL, and the SPIN Investigators. Validation of the Brief Fear of Negative Evaluation Scale‐II in patients with systemic sclerosis: A Scleroderma Patient‐centered Intervention Network Cohort study. Arthritis Care Res. 2018;70(11): 1646-1652.

Mills SD, Kwakkenbos L, Carrier ME, Gholizadeh S, Fox RS, Jewett LR, Gottesman K, Roesch SC, Thombs BD, Malcarne VL, and the SPIN Investigators. Validation of the Social Appearance Anxiety Scale in Patients with Systemic Sclerosis: A Scleroderma Patient-centered Intervention Network Cohort Study. Arthritis Care Res. 2018;70(10):1557-1562.

Carrier M-E, Kwakkenbos L, Boutron I, Welling J, Sauve M, van den Ende C, Schouffoer AA, Hudson M, Thombs BD, Mouthon L, SPIN Investigators. Randomized Feasibility Trial of the Scleroderma Patient-centered Intervention Network Hand Exercise Program (SPIN-HAND): Study Protocol. Journal of Scleroderma and Related Disorders. 2018;3(1):91-97.

Gholizadeh S, Kwakkenbos L, Carrier M-E, Mills SD, Fox RS, Jewett LR, Gottesman K, Roesch S, Thombs BD, Malcarne VL, SPIN Investigators. Validation of the Social Anxiety Interaction Scale (SIAS-6) in systemic sclerosis: A Scleroderma Patient-centered Intervention Network (SPIN) Cohort Study. J Scleroderma Relat Disord. 2018;3(1):98-105.

Jewett LR, Kwakkenbos L, Carrier M-E, Malcarne V, Harcourt D, Rumsey N, Mayes MD, Assassi S, Körner A, Fox RS, Gholizadeh S, Mills SD, Fortune C, Portales A, Thombs BD, SPIN Investigators. Validation of the Body Concealment Scale for Scleroderma (BCSS): Replication in the Scleroderma Patient-centered Intervention Network (SPIN) Cohort. Body Image. 2017;31(20):99-106.

 

Presentations (selected):

Gholizadeh S, Kwakkenbos L, Carrier M-E, Mills SD, Fox RS, Jewett LR, Gottesman K, Roesch SC, Thombs BD*, Malcarne VL. Identifying distinct subgroups of systemic sclerosis patients using body image indicators. 18th National Scleroderma Conference, Calgary, Alberta, September, 2018.

 

Pepin M, Kwakkenbos L, Pelaez S, Carrier M-E, Malcarne VL, El-Baalbaki G, Thombs BD*. Reasons for attending support groups and organizational preferences: the North American Support Group Survey. 5th Annual Skin Research Group of Canada Conference, Montreal, Quebec, Canada, June 2018.

 

Kwakkenbos L, Carrier M-E, Boutron I, Welling J, Sauve M, van den Ende CHM, Schouffoer AA, Hudson M, Thombs BD, Mouthon L, and the SPIN Investigators. Randomized feasibility trial of the Scleroderma Patient-centered Intervention Network Hand Exercise Program (SPIN-HAND). The 5th Systemic Sclerosis World Congress, Bordeaux, France, February 2018.

Rice DB, Cañedo-Ayala M, Carrier M-E, Cumin J, Malcarne V, Hagedoorn M, Thombs BD, & The Caregiver Advisory Committee. Challenges and Service Preferences of Informal Caregivers of People with Systemic Sclerosis. The 5thSystemic Sclerosis World Congress, Bordeaux, France, February 2018.

 

Carrier M-E, Kwakkenbos L, Thombs BD, SPIN Investigators. An International Collaboration to Collect Data and Develop Online Interventions for Scleroderma Patients and an Update from the Scleroderma Patient centered Intervention Network (SPIN). Scleroderma Foundation Annual Patient Conference, New Orleans, Louisiana, USA. July 2016.

 

Carrier M-E, ​Kwakkenbos L, Thombs BD, SPIN Investigators. An International Collaboration to Collect Data and Develop Online Interventions for Scleroderma Patients and an Update from the Scleroderma Patient-centered Intervention Network (SPIN). 4th Systemic Sclerosis World Congress, Lisbon, Portugal. February 2016.

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