- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05221970
Effectiveness and Suitability of the Online Mobile Application for the Mental and Physical Health of Cancer Patients
Effectiveness and Suitability of the Online Mobile Application MOÚ MindCare for the Mental and Physical Health of Cancer Patients: Randomized Controlled Trial
Study Overview
Status
Conditions
Detailed Description
Background: Promoting the mental health of cancer patients is one of the main pillars of comprehensive oncological care. Due to the insufficient capacity of psychotherapists and the mental and physical problems of cancer patients associated with treatment, classical face-to-face mental health support is not always available.
Objectives: 1. To evaluate the impact of online psychological interventions on selected parameters of mental and physical health in cancer patients. 2. To compare which type of psychological intervention is most suitable for which type of oncology patients. 3. To evaluate the moderating roles of intervention adherence and perceived acceptability in the effectiveness of the intervention programs.
Methods: The study design is RCT that includes 4 arms : 1. MBCT (Mindfulness Based Cognitive Therapy) 2. Positive Psychology 3. Autogenic Training 4. Waiting list. Participants will take the 8 week online program via mobile application. Outcomes will be assessed online at, 1) Baseline, 2) Post-intervention (PI), 3) 3 months post PI and 4) 9 months post PI.
Anticipated Findings: Completion of the 8-week online program will lead to the improvement of selected variables of psychological and physical health in oncology patients in comparison with the passive control group. It is expected that programs involving a cognitive component (MBCT-Ca and PP) will be more effective than AT. The investigators expect higher adherence and acceptability to be associated with greater improvement in the outcome variables.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Miroslav Světlák, PhD
- Phone Number: +420 549 49 1372
- Email: msvetlak@med.muni.cz
Study Contact Backup
- Name: Alena Slezáčková, PhD
- Phone Number: +420 604 506 256
- Email: alena.slezackova@med.muni.cz
Study Locations
-
-
Bohunice
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Brno, Bohunice, Czechia, 62500
- Recruiting
- Faculty of Medicine, Masaryk University
-
Contact:
- Miroslav Světlák, PhD
- Phone Number: 549 49 1372
- Email: msvetlak@med.muni.cz
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Men and women over the age of 18
- Diagnosis of some kind of cancer
- Receiving some form of cancer treatment or finished cancer treatment
Exclusion Criteria:
- Patients without a mobil device ("smart" mobile phone)
- Patients without internet access
- Patients suffering from some psychiatric disorder (Schizophrenia, Bipolar Affective Disorder, personality disorder associated with mood changes, Posttraumatic Stress Disorder, suicide attempt, suicide thoughts, Somatoform Disorder or other medically unexplained symptoms which, due to their severity, prevent the person concerned from daily life
- Patients suffering during the last year from: depression with psychotic symptoms, panic anxiety, repeated hospitalization in psychiatry
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Triple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: Waiting list
No intervention.
|
|
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Other: Mindfulness-Based Cognitive Therapy (MBCT-Ca) - online
MBCT uses cognitive behavioral therapy (CBT) methods in collaboration with mindfulness meditative practices and similar psychological strategies.
|
This intervention can be adapted into low-intensity structured program, suitable for eHealth mental health support applications for individual use without the need of direct involvement of a trained mental health professional.
|
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Other: Positive Psychology - online
Positive psychology is focused on the character strengths and behaviors that allow individuals to build a life of meaning and purpose.
|
This intervention can be adapted into low-intensity structured program, suitable for eHealth mental health support applications for individual use without the need of direct involvement of a trained mental health professional.
|
|
Other: Autogenic Training - online
Autogenic training is a relaxation technique focusing on promoting feelings of calm and relaxation to help reduce stress and anxieties.
|
This intervention can be adapted into low-intensity structured program, suitable for eHealth mental health support applications for individual use without the need of direct involvement of a trained mental health professional.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in symptoms of individual stress level using the Perceived Stress Scale
Time Frame: baseline, week 9 from baseline, month 3 post-intervention, month 9 post-intervention
|
The Perceived Stress Scale (PSS) is a classic stress assessment instrument.
The questions in this scale ask about feelings and thoughts during the last month.
Each question has five response options ranging in value from null to four (0=never; 1=almost never; 2=sometimes; 3=fairly often; 4=very often).
To find the total raw score, sum the values of the response to each question (reverse code items 4, 5, 7a and 8).
Individual scores on the PSS can range from 0 to 40 with higher scores indicating higher perceived stress.
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baseline, week 9 from baseline, month 3 post-intervention, month 9 post-intervention
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Change in depression, anxiety and stres using the Depression, Anxiety and Stress Scale
Time Frame: baseline, week 9 from baseline, month 3 post-intervention, month 9 post-intervention
|
The Depression, Anxiety and Stress Scale (DASS-21) is a 21 items scale designed to measure depression, anxiety, and stress.
The instrument comprises three subscales: the emotional states of depression, anxiety, and stress.
Each question has four response options ranging in value from null to four (0= did not apply to me at all; 1= applied to me to some degree, or some of the time; 2= applied to me a considerable degree or a good part of time; 3= applied to me very much or most of the time).
To find the total raw score, sum the values of the response to each question for each of subscale (scores will need to be multiplied by 2 to calculate the final score).
The lowest possible raw score is 0 and the highest possible raw score is 42 for each subscale.
A higher score represents more of the concept being measured.
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baseline, week 9 from baseline, month 3 post-intervention, month 9 post-intervention
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Change in positive mental health using the Positive Mental Health Scale
Time Frame: baseline, week 9 from baseline, month 3 post-intervention, month 9 post-intervention
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The Positive Mental Health Scale (PMHS) is a nine-item scale designed to measure positive mental health (combination of emotional, psychological, and social aspects of well-being).
Each item on the questionnaire is scored from 0 (do not agree) - 3 (agree).
The lowest possible raw score is 0 and the highest possible raw score is 27.
A higher score represents more of the concept being measured.
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baseline, week 9 from baseline, month 3 post-intervention, month 9 post-intervention
|
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Change in health-related quality of life using The Functional Assessment of Chronic Illness Therapy-Spiritual Well-Being
Time Frame: baseline, week 9 from baseline, month 3 post-intervention, month 9 post-intervention
|
The Functional Assessment of Chronic Illness Therapy - Spiritual Well-Being (FACIT)-(Sp) is composed of the FACT-General (FACT-G) and a 12-item Spiritual Well-Being scale (FACIT-Sp-12).The FACT-G (Version 4) is a 27-item compilation of general questions divided into four primary QOL subscales: Physical Well-Being (PWB; 7-items), Social/Family Well-Being (SWB; 7-items), Emotional Well-Being (EWB; 6-items), and Functional Well-Being (FWB; 7-items).Each question has five response options ranging in value from null to four (0= not at all; 1= a little bit; 2=somewhat; 3= quite a bit; 4=very much).
The total FACT-G score is obtained by summing individual subscale scores (PWB + EWB + SWB + FWB).
The lowest possible raw score is 0 and the highest possible raw score is 48 in Spiritual Well-Being subscales.
The lowest possible raw score is 0 and the highest possible raw score is 108 in FACT-G.
A higher score represents more of the concept being measured.
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baseline, week 9 from baseline, month 3 post-intervention, month 9 post-intervention
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Adherence to/satisfaction with the MOÚ MindCare application and intervention programme using the MOÚ MindCare Feasibility Questionnaire
Time Frame: week 9 from baseline
|
Mobile application will be monitoring completing tasks by participants.
Satisfaction with the MOÚ MindCare application will be measured by the MOÚ MindCare Feasibility Questionnaire.
Questions have two, three, four or five response options ranging in value from one to two, three, four or five.
A few questions have open answers options.
To find the total raw score, sum the values of the response to each question (reverse code item: 4).
The lowest possible raw score is 8 and the highest possible raw score is 26.
A higher score represents more of the concept being measured.
|
week 9 from baseline
|
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Change in emotion dysregulation using the Difficulties in Emotion Regulation Scale-SF
Time Frame: baseline, week 9 from baseline, month 3 post-intervention, month 9 post-intervention
|
The Difficulties in Emotion Regulation Scale Short Form (DERS-SF) is a measure used to identify emotional regulation issues.
The measure covers 4 dimensions of emotional regulation: awareness and understanding of emotions; acceptance of emotions; the ability to engage in goal-directed behaviour and refrain from impulsive behaviour when experiencing negative emotions; and access to emotion regulation strategies perceived as effective.
Each question has five response options ranging in value from one to five (1=almost never; 2=sometimes; 3=about half of the time; 4=most of the time; 5=almost always).
The lowest possible raw score is 18 and the highest possible raw score is 90.
A higher score represents more of the concept being measured.
|
baseline, week 9 from baseline, month 3 post-intervention, month 9 post-intervention
|
|
Changes in transdiagnostic and transtheoretical indicators of positive and adaptive functioning using the Five Facet Mindfulness Questionnaire-15
Time Frame: baseline, week 9 from baseline, month 3 post-intervention, month 9 post-intervention
|
The 15-item FFMQ (FFMQ-15) measures five facets: Observing, Describing, Acting with Awareness, Non-Judging of inner experience, and Nonreactivity to inner experience.
Each question has five response options ranging in value from one to five (1=never or very rarely true; 2= rarely true; 3=sometimes true; 4=often true; 5=very often or always true).
To find the total raw score, sum the values of the response to each question (reverse code items 3, 4, 7, 8, 9, 13 and 14).
The lowest possible raw score is 15 and the highest possible raw score is 75.
A higher score represents more of the concept being measured.
|
baseline, week 9 from baseline, month 3 post-intervention, month 9 post-intervention
|
|
Changes in transdiagnostic and transtheoretical indicators of positive and adaptive functioning using the Applied Mindfulness Process Scale
Time Frame: baseline, week 9 from baseline, month 3 post-intervention, month 9 post-intervention
|
The Applied Mindfulness Process Scale (AMPS) measures the application of mindfulness practices in daily life among persons participating in mindfulness-based interventions.
The measure covers three domains of applied mindfulness processes: decentering, positive emotional regulation, and negative emotional regulation.
Each question has five response options ranging in value from null to four (0= never; 1= rarely; 2=sometimes; 3=often; 4=almost always).
To find the total raw score, sum the values of the response to each question.
The lowest possible raw score is 0 and the highest possible raw score is 60.
A score ranging from 0-20 is obtained by summing each factor individually.
A higher score represents more of the concept being measured.
|
baseline, week 9 from baseline, month 3 post-intervention, month 9 post-intervention
|
|
Change in transdiagnostic and transtheoretical indicators of positive and adaptive functioning using the Perceived Hope Scale
Time Frame: baseline, week 9 from baseline, month 3 post-intervention, month 9 post-intervention
|
The Perceived Hope Scale (PHS) is self-report questionnaire measures individual judgment about one's experience and levels of hope.
Each item on the questionnaire is scored from 0-5 (0= strongly disagree, 5= strongly agree).
To find the total raw score, sum the values of the response to each question.
The lowest possible raw score is 0 and the highest possible raw score is 30.
A higher score represents more of the concept being measured.
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baseline, week 9 from baseline, month 3 post-intervention, month 9 post-intervention
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|
Basic personality traits using the Big Five Inventory BFI-10
Time Frame: baseline
|
The Big Five Inventory-10 (BFI-10) measures the Big Five personality traits: Extraversion, Agreeableness, Conscientiousness, Emotional Stability, and Openness.
Each question has five response options ranging in value from one to five (1= disagree strongly; 2= disagree a little; 3= neither agree or disagree; 4= agree a little; 5= agree strongly).
To find the total raw score, sum the values of the response to each question for each of subscale (reverse code items 1,3,4,5 and 7).
The lowest possible raw score is 10 and the highest possible raw score is 50.
A score ranging from 2-10 is obtained by summing each factor individually.
A higher score represents more of the concept being measured.
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baseline
|
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Change in impact of event using the Impact of Event Scale-Revised
Time Frame: baseline, week 9 from baseline, month 3 post-intervention, month 9 post-intervention
|
The Impact of Event Scale - Revised (IES-R) measures impact of recent and specific events, and post-traumatic stress disorder symptoms.
The instrument comprises three subscales: Intrusion; Avoidance and Hyperarousal.
Each question has five response options ranging in value from null to four (0= not at all; 1= a little bit; 2= moderately; 3= quite a bit; 5= extremely).
To find the total raw score, sum the values of the response to each question.
The lowest possible raw score is 0 and the highest possible raw score is 88.
A scores ranging from: 0-32; 0-32 and 0-24 are obtained by summing each factor individually.
A higher score represents more of the concept being measured.
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baseline, week 9 from baseline, month 3 post-intervention, month 9 post-intervention
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|
Change in sleep quality using the Pittsburgh Sleep Quality Index
Time Frame: baseline, week 9 from baseline, month 3 post-intervention, month 9 post-intervention
|
The Pittsburgh Sleep Quality Index (PSQI) measures sleep quality and disturbances.
The instrument comprises seven subscales: subjective sleep quality; sleep latency; sleep duration; habitual sleep efficiency; sleep disturbances; use of sleeping medication and daytime dysfunction.
Questions have four response options ranging in value from null to three and a few questions with open answers options.
To find the total raw score, sum the values of the response to each question and for each subscale separately.
The sum of scores for components yields one global score.
The lowest possible raw score is 0 and the highest possible raw score is 21.
A higher score represents more of the concept being measured.
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baseline, week 9 from baseline, month 3 post-intervention, month 9 post-intervention
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Change in fatigue using the Fatigue Symptom Inventory
Time Frame: baseline, week 9 from baseline, month 3 post-intervention, month 9 post-intervention
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The Fatigue Symptom Inventory (FSI) measures multiple aspects of fatigue, including its perceived severity, frequency, and interference with daily functioning.
Each item on the questionnaire is scored from 0-10 (0= not at all fatigued, 10= as fatigued as I could be).
To find the total raw score, sum the values of the response to each question.
The lowest possible raw score is 0 and the highest possible raw score is 130.
A higher score represents more of the concept being measured.
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baseline, week 9 from baseline, month 3 post-intervention, month 9 post-intervention
|
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The total amount of received health care using the medical documentation software (GreyFox)
Time Frame: month 9 post-intervention
|
Number of PET, CT and MR imaging examinations, number of acute hospitalizations, the total cost of care, and the type and amount of anticancer treatment will be measured by using hospital database program called "GreyFox".
|
month 9 post-intervention
|
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Changes in severity of somatic symptoms using the Patient Health Questionnaire 15
Time Frame: baseline, week 9 from baseline, month 3 post-intervention, month 9 post-intervention
|
The Patient Health Questionnaire (PHQ-15) measures common mental disorders and is used to assess somatic symptom severity and screen for the potential somatisation and somatoform disorders.
Each question has three response options ranging in value from null to two (0= not bothered at all; 1= bothered a little; 2= bothered a lot).
To find the total raw score, sum the values of the response to each question.
The lowest possible raw score is 0 and the highest possible raw score is 30.
A higher score represents more of the concept being measured.
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baseline, week 9 from baseline, month 3 post-intervention, month 9 post-intervention
|
|
Change in pain medication use
Time Frame: baseline, week 9 from baseline, month 3 post-intervention, month 9 post-intervention
|
The following variables about medication will be collected: name and strength of medication; number of days in the week the medication was taken (0-7), number of taken doses per the day (0-7 and more); regularity of a medication using (options: regularly/according to need).
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baseline, week 9 from baseline, month 3 post-intervention, month 9 post-intervention
|
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Change in psychiatric medication use
Time Frame: baseline, week 9 from baseline, month 3 post-intervention, month 9 post-intervention
|
The following variables about medication will be collected: name and strength of medication; condition the medication is used for (options= sleep disorder/anxiety/depression/other); number of days in the week the medication was taken (0-7); number of taken doses per the day (0-7 and more); regularity of a medication using (options: regularly/according to need).
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baseline, week 9 from baseline, month 3 post-intervention, month 9 post-intervention
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|
Change in pain intensity using the Numerical Rating Scale of Pain Intensity
Time Frame: baseline, week 9 from baseline, month 3 post-intervention, month 9 post-intervention
|
Pain intensity will be measured by the Numerical Rating Scale of Pain Intensity (NRS-I) consists of a range of numbers (0-10).
The lowest number is null and represents "no pain".
The highest number is ten and represents "an extreme level of pain".
Respondents are asked to choose the number that best represents a level of pain intensity.
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baseline, week 9 from baseline, month 3 post-intervention, month 9 post-intervention
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|
Change in dealing with pain using the Pain Self-Efficacy Questionnaire
Time Frame: baseline, week 9 from baseline, month 3 post-intervention, month 9 post-intervention
|
The Pain Self-Efficacy Questionnaire is a 10-item scale designed to measure the confidence of people with ongoing pain to achieve different activities despite pain.
Each item on the questionnaire is scored from 0 (not at all confident) to 6 (completely confident).
The lowest possible raw score is 0 and the highest possible raw score is 60.
A higher score represents more of the concept being measured.
|
baseline, week 9 from baseline, month 3 post-intervention, month 9 post-intervention
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|
Change in current emotional state using the Self-Assessment Manikin
Time Frame: during a whole intervention (3 times a day)
|
Current emotional state will be assessed three times per day using three short items (Self-Assessment Manikin) directly incorporated in the MOÚ MindCare Application.
The Self-Assessment Manikin (SAM) measures pleasure, arousal, and dominance.
It is a non-verbal pictorial assessment technique.
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during a whole intervention (3 times a day)
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Changes in transdiagnostic and transtheoretical indicators of positive and adaptive functioning using the Self-Compassion Scale
Time Frame: baseline, week 9 from baseline, month 3 post-intervention, month 9 post-intervention
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The Self-compassion Scale (SCS) is a psychometrically measurement of self-compassion.
The instrument comprises six subscales: Self-Kindness; Self-Judgment; Common Humanity; Isolation; Mindfulness and Over-identification.
Each item on the questionnaire is scored from 1-5 (1=almost never, 5=almost always).
To find the total raw score, sum the values of the response to each question for each of subscale (reverse code items 1, 2, 4, 6, 8, 13, 16, 18, 20, 21, 24 and 25).
The lowest possible raw score is 26 and the highest possible raw score is 130.
A higher score represents more of the concept being measured.
|
baseline, week 9 from baseline, month 3 post-intervention, month 9 post-intervention
|
|
Changes in transdiagnostic and transtheoretical indicators of positive and adaptive functioning using the Gratitude Questionnaire Six-Item Form
Time Frame: baseline, week 9 from baseline, month 3 post-intervention, month 9 post-intervention
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The Gratitude Questionnaire-Six-Item Form (GQ-6) is a self-report questionnaire measures individual differences in the proneness to experience gratitude in daily life.
Each question has seven response options ranging in value from one to seven (1= strongly disagree; 2= disagree; 3= slightly disagree; 4= neutral; 5= slightly agree; 6= agree; 7= strongly agree).
To find the total raw score, sum the values of the response to each question (reverse code items 3 and 6).
The lowest possible raw score is 6 and the highest possible raw score is 42.
A higher score represents more of the concept being measured.
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baseline, week 9 from baseline, month 3 post-intervention, month 9 post-intervention
|
|
Change in rumination and reflection using the Rumination-Reflection Questionnaire
Time Frame: baseline, week 9 from baseline, month 3 post-intervention, month 9 post-intervention
|
The Rumination Reflection Questionnaire (RRQ) measures an adaptive (self-focus) and maladaptive form (self-rumination) of self-focus or self-attention.
The instrument comprises two subscales: Rumination and Reflection.
Each question has five response options ranging in value from one to five (1= strongly disagree; 2= disagree; 3= neutral; 4= agree; 5= strongly agree).
To find the total raw score, sum the values of the response to each question for each of subscale (reverse code items 6, 9, 10, 13, 14, 17, 20 and 24).
The lowest possible raw score is 24 and the highest possible raw score is 120.
A score ranging from 12-60 is obtained by summing each factor individually.
A higher score represents more of the concept being measured.
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baseline, week 9 from baseline, month 3 post-intervention, month 9 post-intervention
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Socio-demographic variables
Time Frame: baseline
|
The following socio-demographic variables will be collected: gender, age, level of education, marital status, number of children (if any), employment status, any previous experience with autogenic training, psychotherapy, meditation, or another practice of self-development (how long/ how often is one practicing such activities).
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baseline
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Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Study Chair: Miroslav Světlák, PhD, Masaryk university
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 2022NALET
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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