Ce portail, réservé aux membres de la SCP seulement, a été créé afin de permettre aux membres de la SCP d’afficher des demandes pour que d’autres membres de la SCP servent de participants dans leurs études de recherche.
Pour afficher votre projet vous devez nous en fournir une brève description, indiquant qui vous cherchez à recruter, l’obligation des participants et la durée de la collecte de données.
Pour plus d’informations, reportez-vous au Portail de recrutement de participants à la recherche, qui décrit le processus de proposition.
Description: BACKGROUND: Recent evidence shows that sleep disturbance can predict the severity of eating disorder (ED) symptoms. This link suggests that improving sleep problems in ED populations is a viable pathway to improving ED symptoms. Cognitive behavioural therapy for insomnia (CBT-I) is the first-line treatment for sleep disturbance in psychiatric populations. Before introducing CBT-I to a new population, it is critical that it is adapted to the sleep-related thoughts and behaviours unique to that population. PROBLEM: Sleep-related thoughts and behaviours unique to ED populations remain unknown. PURPOSE: The present study assesses sleep-related thoughts and behaviours in ED populations to inform the development and initial feasibility of a behaviourally-based sleep intervention tailored specifically to ED populations. METHODS: A mixed-methods explanatory sequential design will be used, which includes an online survey followed by a virtual focus group. The study is shared via multiple media platforms dedicated to eating disorder awareness and recovery. We are recruit females, aged 18–50 years, and who report co-occurring insomnia and eating disorder symptoms. DATA ANALYSIS: The quantitative data will be analyzed using Statistical Package for the Social Sciences (SPSS, Version 25) and the qualitative data will be analyzed using thematic analysis
Specifics: Study Population:
Participants: Females, aged 18-50 years, who are not pregnant, and who are currently experiencing eating disorder symptoms and sleep disturbance.
Regional population: North America.
Sample size: Survey (N=200) and focus group (N=6). Participant Obligation:
Obligation: online informed consent and survey with questions on thoughts and behaviours related to sleep and eating.
Optional: Express interest in participating in the focus group.
Description: The purpose of this study is to assess the utility of different levels of communication in intimate partner violence risk assessments. All participants receive complimentary access to a 1-hr webinar on intimate partner violence risk assessment and management presented by Dr. P. Randall Kropp and offered online through CONCEPT at Palo Alto University, a leading CE provider for mental health and other human service professionals - a USD $100 value!
Specifics: Study Population:
Mental health professionals, law enforcement officers, and victim service workers involved in the assessment and management of intimate partner violence who are fluent in English.
Participants will be asked to complete an anonymous, online survey that will take approximately 30 to 60 minutes.
Location: Online – British Columbia
Project lead: Mehrnaz Peikarnegar, Supervisor: Dr. Stephen D. Hart
Description: The purpose of this survey is to better understand how psychologists conduct suicide risk assessments and how the practice affects them. The goal is to use these data to inform suicide risk assessment training, practice, and policy in Canada.
Specifics: Study Population
This study is open to individuals who are:
(a) registered/licensed psychologists currently practicing in Canada AND
(b) have completed suicide risk assessments with clients/patients in the last 10 years.
In this study, you will be asked questions about your suicide risk assessment practices, training, and experiences, as well as demographics at the end.
This anonymous survey is expected to take 20-30 minutes to complete.
Location: Online - Edmonton
Project lead: Jonathan Dubue, Supervisor: Phillip Sevigny
Description: The purpose of this study is to better understand the bicultural experience of first- and second-generation immigrants of South Asian descent; particularly, gender perceptions apparent in the interaction of both cultures: Canadian vs South Asian.
Specifics: Study Population:
To participate in this study, you must be South Asian (from India, Pakistan, Bangladesh, Nepal, Sri Lanka, Kashmir, Maldives, Bhutan, and Afghanistan) and either born outside of Canada or born in Canada with parents born outside of Canada.
You will be asked to label some icons and symbols and complete a word search puzzle. You will then be asked to answer questions regarding your ethnicity, language, and gender. This study will take less than 50 minutes to complete.
Location: Online - Edmonton.
Project lead: Ramanjot Kalher, Supervisor Dr. Kimberly Noels
Description: The Social Tech and Physical Distance Study 2021 is an online survey study about people using technologies to connect with others while the COVID-19 physical distancing measures are in place during North American Winter 2021. Are you 18 or older? Read English well or very well? Then you can participate! Get to the survey here: http://uottawapsy.az1.qualtrics.com/jfe/form/SV_7NDScpjPGhbBFZQ If you have any questions or comments, please send an email to Dr. Shaughnessy at firstname.lastname@example.org. Thank you for your interest!
Specifics: Study Population:
Individuals 18 years and older who speak English well or very well
Complete a 20 minute online survey
Description: Posttraumatic Stress Disorder (PTSD) will be a severe problem in Canada in the wake of COVID-19, especially for Military Members, Veterans, First Responders, and Healthcare Workers (MVFH). However, gold standard face-to-face PTSD treatments do not meet current MVFH needs, which requires virtual interventions and minimal healthcare resources. Recognizing the need for a virtual, low-resource PTSD intervention for MVFH with PTSD and their loved ones, the investigators developed Couple HOPES (Helping Overcome PTSD and Enhance Satisfaction). Couple HOPES is a secure, online self-help intervention for those with PTSD and their partners. However, MVFH are now particularly likely to be exposed to traumas related to COVID-19. It is essential to identify if Couple HOPES is safe and helpful for couples involving MVFH with COVID-19-related PTSD specifically. This project will therefore test the efficacy of Couple HOPES compared to a delayed waitlist control in 140 couples wherein one member is a MVFH with PTSD, half of whom have COVID-19-related PTSD. The investigators will examine if Couple HOPES is helpful in improving PTSD symptoms and relationship satisfaction for such couples, and if it is more or less helpful to this end for these couples compared to those with other forms of trauma exposure.
Specifics: Study Population:
The study population includes couples that have at least one member of the couple who is a service member, veteran, first responder, or healthcare worker with significant symptoms of PTSD.
Both members of the couple must be willing to do intervention modules together, have a computer and access to high-speed Internet, have brief phone calls with a “coach” to help them use the online program, and complete online questionnaires.
Description: The purpose of this project is to examine self-care, stress, and wellbeing amongst trainees in professional psychology graduate programs.
Specifics: Study Population: All graduate students in professional psychology programs (e.g., clinical, counselling, school, clinical neuropsychology) are welcome to participate.
Participant Obligation: Participation in this study consists of the completion of a 20 minute questionnaire via SurveyMonkey regarding your (a) current self-care behaviours and (b) stress and wellbeing.
Description: The purpose of this dissertation research study is to understand what it is like to be a psychologist working in or commuting to rural communities when they are not originally from the community and to explore how they experience developing helpful relationships with rural clients. This study also explores what it is like to be a rural client receiving services in their community from a psychologist not originally from their community and what it is like to develop a therapeutic relationship with that provider. Research holds that the therapeutic alliance is key to successful outcomes but that developing relationships in rural communities may be more difficult, especially for outsider providers. For the purpose of this recruitment phase, the researcher is inviting CPA members to nominate a rural psychologist who you believe is successful in rural practice and who is registered with the College of Alberta Psychologists, to be a participant in this study. To nominate a rural psychologist practicing in Alberta, please send their publicly available information (i.e., work contact) to Laura Friesen at Lsfriese@ualberta.ca. Nominated psychologists will then be contacted and invited to participate in this study. Nominator information will not be shared with potential participants and participants may freely choose to participate with no negative consequences should they opt out
Specifics: Study Population: This study is inviting individuals to nominate a Registered Psychologist who is registered and working in Alberta, who has at least one year of experience living and working in or commuting to rural communities when they are not from that community.
Participant Obligation: Participants in this study will be asked to take part in an online video (Zoom 5.0) interview. Two interviews may be needed to complete the interview. Participants will be asked to complete several simple pre-interview activities (PIAs).
Location: This study will be conducted online - Edmonton and will recruit participants across Alberta, Canada.
Project lead: Laura Friesen, Supervisor: Dr. Sophie Yohani
Description: The objective of this two-phase study is to examine the relationship between coping responses to everyday challenges and wellbeing. For phase 1, participants will complete an online questionnaire. The online questionnaire will ask participants questions about their mental health status (e.g., anxiety, depression, post-traumatic stress symptoms) and how they cope with negative life events or challenges. The second phase of the study will consist of completing daily expressive writing activities for seven consecutive days. Participants will be asked to reflect on things that occurred earlier that day, while following guides to help them reflect on these events. The second phase of the study will also consist of completing three follow-up online questionnaires (2 weeks, 1 month, and 3 months after completing the writing program). Enrolment in phase 2 of the study requires the completion of the online questionnaire for phase 1. If participants are interested in enrolling in phase 2, they will have the opportunity to provide us with their email address to commence phase 2. This study has received ethical approval by the ethics board at the University of Ottawa.
Specifics: Study Population: Seeking individuals who are 16 years or older who can read and write well in English and who identify as ethnic minorities (e.g., Black/African-Canadians, Indigenous Canadians, East Asians) to partake in a two-part study.
Participant Obligation: It will take participants one hour to complete phase 1. For phase 2, it will take participants 10-15 minutes per day for seven days, in addition to four follow-up surveys that will each take one hour to complete.
Location: Online - Ottawa
Project lead: Kayla Boileau, Supervisor: Dr. Andra Smith
Description: The aim of this survey is to better understand how the coronavirus and the impact the current lockdown is having on our day to day lifestyle. We hope to find out what is helpful for people during this time and also what may be causing some people to be affected more than others in terms of their wellbeing. NOTE: This is the 2nd wave of this survey - if you completed the 1st wave of this survey study in September/October 2020, you are very welcome to also complete the 2nd wave! We also hope that those who missed our 1st survey will consider completing this 2nd one! Collecting information on your current experiences will be helpful in comparing the experiences of Canadians earlier on in the pandemic to experiences more recently.
Specifics: Study Population: This study is open to individuals living in Canada who are 17 years of age or older.
Participant Obligation: To participate in this study, you will be asked to complete an online survey which will take approximately 15 minutes. It can be completed on most browsers on most devices, including mobile devices.
Description: Due to the COVID-19 pandemic, health care workers face highly stressful and rapidly changing work environments. Mental health concerns in the population have also increased (e.g., isolation, anxiety, substance use), but accessing mental health services is more difficult. Mental health clinicians face increased demands and substantial stress; it is critical to understand their experiences to ensure the availability of high-quality services, including those using telehealth technologies like videoconferencing. This study uses online surveys in 6 languages (including French and English) to assess the impact of the COVID-19 pandemic on clinical practice and well-being of global mental health professionals. Surveys will be implemented at three time points to asses changes over time; the first has been completed. Participants will be members of the World Health Organization’s Global Clinical Practice Network, including 15,500 mental health clinicians from 159 countries. The study assesses: 1) Effects of COVID-19 on work circumstances and services provided; 2) Work-related stress and distress; 3) Use of telehealth services and related concerns; and 4) Expectations, resource needs, and recommendations. Results will inform clinical and health system management and public health response. Findings will be crucial for developing policies to protect the mental health workforce in Canada.
Specifics: Study Population:
Seeking registered psychologists in Canada. Participants are asked to join the Global Clinical Practice Network (GCPN; website link below).
Once a GCPN profile is set up, in October 2020 and March 2021, members will be invited via email to participate in a 30-minute COVID-19 survey. For questions, please email email@example.com.
Description: The primary aim of the proposed study is to examine the complex interplay between multiple self, peer, and family variables relative to the development of anxiety symptoms in females. The literature has provided an abundance of evidence to suggest that anxiety related issues and symptoms in adolescence predominately reside in females. Due to these sex differences in anxiety symptom severity during this developmental period, the current study aims to focus on examining the abovementioned variables in a female population. The rationale for developing the proposed model is based on bodies of literature, including (1) developmental psychopathology perspective and cognitive-behavioural theory of anxiety disorders; (2) etiological perspectives of anxiety disorders in youth; (3) research on youth’s emotional distress (i.e., associated cognitive, behavioural, and physiological symptoms), peer relationships, parents anxiety symptoms, and parenting behaviours. The goal of the proposed research is to move towards conceptualizing the development of anxiety symptoms through multiple variables, rather than isolated factors. This examination has the potential to enhance the scientific understanding of the development of sub-clinical anxiety symptoms in youth.
Specifics: Study Population: Female youth aged 11 to 18 and their parents. Individuals can choose to participate if they experience(d) current/past diagnoses or medical conditions, take prescribed medications, and live in any city or province within Canada.
Participant Obligation: Complete a series of questionnaires via Qualtrics.
Location: Online City - Calgary, AB
Project lead: Victoria Purcell, Supervisor: Jac J.W Andrews
Description: This two phase study examines the relationship between personality characteristics and life circumstances on coping responses to the 2019 Coronavirus (phase 1). Additionally, this study examines the impact of tailored expressive writing exercises on processing and coping with challenges posed by COVID-19 (phase 2). This study requires the complete of an online survey (phase 1), daily writing activities/reflections, and follow-up surveys (phase 2). Compensation is provided for phase 2, such that each writing activity completed corresponds to an additional chance to win one of four money prizes.
Specifics: Study Population: Seeking individuals who are 17 years or older who can read and write well in English.
Participant Obligation: Completing an online survey (phase 1, 30-40 minutes), daily writing activities for fourteen consecutive days (10-15 minutes each), and completion of follow-up surveys at 2 weeks, 1 month, and 3 months after the writing activities (phase 2).
Description: Une étude récente, menée auprès de psychologues canadiens, a révélé que les indicateurs de suivi de progrès en thérapie sont encore peu connus et peu utilisés par les psychologues francophones (Ionita & Fitzpatrick, 2014). En effet, par comparaison aux anglophones, les cliniciens francophones sont moins conscients de l’existence de ces mesures et les utilisent significativement moins dans leur pratique. Une des raisons expliquant l’existence de cette différence est le fait que plusieurs de ces indicateurs de suivi de progrès ne sont pas disponibles en français. L’objectif général de ce programme de recherche est de combler ces lacunes en traduisant et en validant, en français, diverses mesures d’indicateurs de suivi de progrès en thérapie.
Study Population: Les critères d’inclusion des participants sont les suivants : être âgé de 18 ans et plus, être francophone et être en début de psychothérapie. Nous recrutons des participants qui proviennent du Nouveau-Brunswick et de l’extérieur de la province.
Participant Obligation: La tâche des participants est de remplir une série de questionnaires après leur 1ere séance, 4e séance et 8e séance de thérapie. La série de questionnaires prend environ une heure à compléter et peut être remplie au domicile du participant.
Les participants recevront une compensation monétaire de 20$ après chaque temps de mesure.
Les coûts de livraison des questionnaires sont assumés par les chercheurs.