Depressive Symptoms Clinical Trial
— CROPOfficial title:
Cultivating Resilience in Oncology Practice: A Feasibility Study of Pediatric Patients
The purpose of the CROP study is to investigate the potential to cultivate psychological resources and resilience in childhood cancer patients and their family members using a mobile phone-based intervention. The feasibility study aims to evaluate the implementation and participant experience of the digital intervention and register psychological outcome measures preliminary evidence for its acceptability, feasibility, and potential beneficial effects.
Status | Not yet recruiting |
Enrollment | 40 |
Est. completion date | May 2, 2023 |
Est. primary completion date | December 31, 2022 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 10 Years to 18 Years |
Eligibility | Inclusion Criteria: - Newly diagnosed cancer - Chronic pediatric disease Exclusion Criteria: - Severe crisis reaction - Late-stage palliative care - Severe intellectual disability - Psychiatric disease hindrance - Participation in other study with psychological intervention |
Country | Name | City | State |
---|---|---|---|
Sweden | H.K.H. Crown Princess Victoria Children's Hospital, Linköping University Hospital, Sweden | Linköping |
Lead Sponsor | Collaborator |
---|---|
Linkoeping University |
Sweden,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Mental Health Continuum-Short Form (MHC-SF) | 14 items. Score (min-max): 0-70. A high score indicates mental well-being. | At the beginning of the trial. | |
Primary | Mental Health Continuum-Short Form (MHC-SF) | 14 items. Score (min-max): 0-70. A high score indicates mental well-being. | After 12 weeks of participation in the trial. | |
Primary | Mental Health Continuum-Short Form (MHC-SF) | 14 items. Score (min-max): 0-70. A high score indicates mental well-being. | At 12-month after completion of the trial. | |
Secondary | Strengths and Difficulties Questionnaire (SDQ) | 25 items. Score (min-max): 0-25. A high score indicates psychiatric difficulties. | At the beginning of the trial. | |
Secondary | Strenghs and Difficulties Questionnaire (SDQ) | 25 items. Score (min-max): 0-25. A high score indicates psychiatric difficulties. | After 12 weeks of participation in the trial. | |
Secondary | Strengths and Difficulties Questionnaire (SDQ) | 25 items. Score (min-max): 0-25. A high score indicate psychiatric difficulties. | At 12-month after completion of the trial. | |
Secondary | Revised Child Anxiety and Depression Scale Short form (RCADS-SF) | 25 items. Score (min-max): 0-75. A high score indicates symptoms of anxiety and depression. | At the beginning of the trial. | |
Secondary | Revised Child Anxiety and Depression Scale (RCADS) | 25 items. Score (min-max): 0-75. A high score indicates symptoms of anxiety and depression. | After 12 weeks of participation in the trial. | |
Secondary | Revised Child Anxiety and Depression Scale (RCADS) | 25 items. Score (min-max): 0-75. A high score indicates symptoms of anxiety and depression. | At 12-month after completion of the trial. | |
Secondary | System Usability Scale (SUS) | 10 items. Score (min-max): 10-50. A high score indicates a high level of usability. | After completion of the 12 week trial. |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT02909387 -
Adapting Project UPLIFT for Blacks in Georgia
|
N/A | |
Completed |
NCT05702086 -
Making SPARX Fly in Nunavut: Pilot Testing an E-intervention for Boosting Resilience Against Youth Depression
|
N/A | |
Terminated |
NCT04921332 -
Bright Light Therapy for Depression Symptoms in Adults With Cystic Fibrosis (CF) and COPD
|
N/A | |
Completed |
NCT03535805 -
Transdiagnostic, Cognitive and Behavioral Intervention for in School-aged Children With Emotional and Behavioral Disturbances
|
N/A | |
Recruiting |
NCT06100146 -
Effectiveness of Fortification With Folic Acid and Vitamin B12 Among Teenage Girls
|
N/A | |
Recruiting |
NCT03272230 -
Assessment of Apathy in a Real-life Situation, With a Video and Sensors-based System
|
N/A | |
Completed |
NCT03514355 -
MBSR in Rheumatoid Arthritis Patients With Controlled Disease But Persistent Depressive Symptoms
|
N/A | |
Completed |
NCT05376397 -
Testing THRIVE 365 for Black Sexual Minority Men (On The Daily)
|
N/A | |
Terminated |
NCT04367636 -
The Effects of Attention Training on Emotion Regulation and Stress Related Complaints During COVID-19
|
N/A | |
Completed |
NCT04403126 -
To Increase Psychological Well-being by the Implementation of Forgiveness Education
|
N/A | |
Recruiting |
NCT05078424 -
Cognitive Behavioural Therapy for Youths With Depressive and Anxiety Symptoms in Hong Kong
|
N/A | |
Recruiting |
NCT06053775 -
Non-Invasive Brain Stimulation and Cognitive Training for Depressive Symptomatology Related to Breast Cancer (ONCODEP)
|
N/A | |
Active, not recruiting |
NCT04084795 -
Augmentation of EMDR With tDCS in the Treatment of Fibromyalgia
|
N/A | |
Recruiting |
NCT04082052 -
Evaluating and Predicting Response to a Single Session Intervention for Self-Dislike
|
N/A | |
Completed |
NCT04011540 -
Digital Data in Mental Health Therapy
|
N/A | |
Not yet recruiting |
NCT06413849 -
Telephone-coached "Graphic Narrative" Bibliotherapy for Dementia Caregivers
|
N/A | |
Not yet recruiting |
NCT03659591 -
Triple Aim Psychotherapy: Aimed at Improving Patient Experience, Population Health, and Cost
|
N/A | |
Not yet recruiting |
NCT02133170 -
"Mindfulness vs Psychoeducation in Bipolar Disorder"
|
N/A | |
Completed |
NCT02314390 -
Group- Versus Individual-Mindfulness-Based Cognitive Therapy: a Randomized Trial
|
N/A | |
Completed |
NCT01628016 -
The Effect of Attention Bias Modification Training on Reducing Depressive Symptoms
|
N/A |