The Use of Humor With Young Adults in Psychiatric Care
NCT04778163 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 34
Last updated 2022-11-01
Summary
Clinical study in psychiatry in young adult patients between 18 and 25 years old. The aim of the study is to evaluate the therapeutic impact of the clinical use of humor through 6 group sessions (group of 5 to 10 patients), at the rate of one hour session per week for 6 weeks.
The investigators will form 2 groups of 5 to 10 patients matched in terms of gender, education level and score on a scale measuring their sense of humor. The participants will be asked to complete a series of tests measuring their ability to use humor, psychiatric symptoms and well-being.
Group 1 (test group) will participate in the humor-based sessions, while Group 2 (control group) will receive regular treatment for 6 weeks (waiting list: patients in Group 2 will attend humor-based sessions once Group 1 has completed their 6 weeks).
At the end of the 6-week sessions, both groups will receive the same series of pre-session tests to see whether or not there has been improvement in their overall functioning, psychiatric symptomatology and appreciation/use of humor.
At the end of the 2x 6-week sessions, group 2 will again receive this series of pre-session tests to see whether or not their overall functioning, psychiatric symptomatology and appreciation/use of humour has improved.
Objective(s)/Aim:
To evaluate the resilience of young adult psychiatric patients and their ability to cope with stress through the use of humor in a set of 6 modules on the use of humor.
To evaluate the symptoms.
Outcome/Endpoints :
Using scales, measure this evolution.
Conditions
- Treatment Adherence and Compliance
- Psychiatric Disorder
Interventions
- BEHAVIORAL
-
Clinical use of humor
Clinical study in psychiatry in young adult patients between 18 and 25 years old. The aim of the study is to evaluate the therapeutic impact of the clinical use of humor through 6 group sessions (group of 5 to 10 patients), at the rate of one hour session per week for 6 weeks. The investigators will form 2 groups of 5 to 10 patients matched in terms of gender, education level and score on a scale measuring their sense of humor. The participants will be asked to complete a series of tests measuring their ability to use humor, psychiatric symptoms and well-being.
Sponsors & Collaborators
-
University Hospital, Geneva
lead OTHER
Principal Investigators
-
Cédric AM Devillé, Dr · University Hospital, Geneva
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Max Age
- 25 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2019-09-19
- Primary Completion
- 2022-06-30
- Completion
- 2022-10-31
Countries
- Switzerland
Study Locations
More Related Trials
-
Mechanisms of Change in Brief Treatment for Borderline Personality Disorder
NCT03717818 ·Status: UNKNOWN ·Phase: NA
-
Psychiatric Future of Young Patients Hospitalized in the Pass'Aje Service Between 2006 and 2010
NCT03309670 ·Status: UNKNOWN
-
Targeting Burdensomeness Among Clinic Referred Youth
NCT03781037 ·Status: COMPLETED ·Phase: NA
-
Psychosocial Group Interventions for Depression
NCT02149381 ·Status: COMPLETED ·Phase: NA
-
Outcomes From Remediation and Behavioural Intervention Techniques
NCT05731414 ·Status: RECRUITING ·Phase: NA
-
Cognitive Behavioral Therapy for the Prevention of Paranoia in Adolescents at High Risk
NCT01923701 ·Status: COMPLETED ·Phase: NA
-
Psychological Prevention of Internalizing Disorders
NCT00564239 ·Status: COMPLETED ·Phase: NA
-
The Feasibility of a Novel Intervention for At Risk Mental State
NCT03160092 ·Status: UNKNOWN ·Phase: NA
-
Cognitive Behavioral Therapy for Patients With an Early Psychosis
NCT01511406 ·Status: COMPLETED ·Phase: PHASE2
-
Intervention Targeting Depressive Symptoms and Mental Rumination
NCT04595539 ·Status: UNKNOWN ·Phase: NA
-
Motivational Interviews for Depression in Primary Care
NCT01114334 ·Status: COMPLETED ·Phase: NA
-
Effectiveness and Equivalence of an Internet-based Virtual Classroom Intervention for Psychosomatic Aftercare
NCT04989842 ·Status: COMPLETED ·Phase: NA
-
Testing Psychosocial Treatment Planning Methods for Youth Anxiety and Depression
NCT03610373 ·Status: COMPLETED ·Phase: NA
-
Efficacy of Transitional Case Management Following Psychiatric Hospital Discharge
NCT02258737 ·Status: COMPLETED ·Phase: NA
-
An Electronic Intervention to Reduce Cannabis Among Young Adults in Psychiatric Care
NCT04174963 ·Status: TERMINATED ·Phase: NA
-
Skills for Wellness
NCT01980147 ·Status: RECRUITING ·Phase: NA
-
Treatment of Anxiety in Late Adolescents With Autism
NCT02977962 ·Status: UNKNOWN ·Phase: NA
-
Treating Self-criticism in Adolescents: a Study With Single-case Experimental Design
NCT05247190 ·Status: COMPLETED ·Phase: NA
-
Study of the Transition From Child Psychiatry to Adult Psychiatry in Nice Within a Population of 17-year-old Adolescents
NCT07068945 ·Status: NOT_YET_RECRUITING
-
Efficacy and Mechanisms of Change of an Emotion-oriented Version of Cognitive-behavioral Therapy for Psychosis
NCT02787135 ·Status: COMPLETED ·Phase: NA
-
A School-Based Intervention to Reduce Stigma & Promote Mental-Health Service Use
NCT03597048 ·Status: COMPLETED ·Phase: NA
-
Single Session Intervention to Prevent Common Mental Disorders and Among College Students
NCT04267068 ·Status: COMPLETED ·Phase: NA
-
Group Psychotherapy in Long COVID
NCT06726772 ·Status: COMPLETED ·Phase: NA
-
Caregiver Stress and Sleep Study
NCT05219955 ·Status: RECRUITING ·Phase: NA
-
Implementation of a Psychological Online Intervention for Low to Moderate Depression in Primary Health Care
NCT05294614 ·Status: UNKNOWN ·Phase: NA