Depression Clinical Trial
Official title:
Recovery and Rehabilitation After Lung Cancer Surgery
NCT number | NCT01399541 |
Other study ID # | 59081001 |
Secondary ID | |
Status | Completed |
Phase | |
First received | |
Last updated | |
Start date | October 2010 |
Est. completion date | April 2018 |
Verified date | August 2018 |
Source | Oslo University Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
The specific aims of this translational, interdisciplinary, multi-center, international
research study with 300 Lung cancer patients are to:
Aim 1 Explore how the patients experience the transfer between different locations and
between different levels of care at the same location and how they experienced coming home.
Aim 2 Explore lung cancer patients' symptoms, symptom clusters, and changes in symptoms and
symptom clusters over time.
Aim 3 Explore interaction between lung cancers patients' symptoms, symptom clusters, health
related quality of life and social support.
Status | Completed |
Enrollment | 300 |
Est. completion date | April 2018 |
Est. primary completion date | April 2014 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - patients with lung cancer patients above the age of 18 that have been treated with surgery, who are able to speak and understand Norwegian, Exclusion Criteria: - and who suffer no cognitive impairment. |
Country | Name | City | State |
---|---|---|---|
Norway | Haukeland Sykehus | Bergen | |
Norway | Rikshospitalet, OUS | Oslo | |
Norway | Ullevaal University Hospital | Oslo | |
Norway | St. Olavs Hospital | Trondheim |
Lead Sponsor | Collaborator |
---|---|
Oslo University Hospital | St. Olavs Hospital, Ullevaal University Hospital |
Norway,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Key measures that will be the focus of the study is Quality of life. | Data will be collecetd using the self administered questionnaire: EORTC QLQ-C30 + LC13 | 1 year with 5 measurement points | |
Secondary | The total burden of symptoms will be one key measures in this observational study. | The self administered questionnaire: Memorial Assessment scale (MSAS) Key measures that will be used to evaluate the intervention(s) or, for observational studies, that are a focus of the study. | one year with 5 measuresments | |
Secondary | A key measure to measure fatigue will be used. | The self administered questionnaire: Lee Fatigue Scale, LFS. Key measures that will be used to evaluate the intervention(s) or, for observational studies, that are a focus of the study. | one year with five measurements points | |
Secondary | A key measures to measure sleep disturbances will be used. | A questionnaire: General sleep disturbances scale (GSDS). Key measures that will be used to evaluate the intervention(s) or, for observational studies, that are a focus of the study. | One year with five measurements points | |
Secondary | A key measures will be used to evaluate social support | The self administered questionnaire: Social Provision Scale. Key measures that will be used to evaluate the intervention(s) or, for observational studies, that are a focus of the study. | One year with two measurements points | |
Secondary | A self administered questionnaire to measure Anxiety | The self administered questionnaire: State and trait anxiety (STAI). Key measures that will be used to evaluate the intervention(s) or, for observational studies, that are a focus of the study. | One year with five measurements points | |
Secondary | A self administered questionnaire to measure pain | The self administered questionnaire: Brief Pain Inventory. Key measures that will be used to evaluate the intervention(s) or, for observational studies, that are a focus of the study. | one year with five measurements points | |
Secondary | Depression is a key measure | The self administered questionnaire: Self-report depression scale (CES-D). Key measures that will be used to evaluate the intervention(s) or, for observational studies, that are a focus of the study. | One year with five measurements points | |
Secondary | One key measures that will be used to evaluate stigma related to having lung cancer in this observational study. | Data will be collected using the self administered questionnaire: Cataldo Lung Cancer Stigma Scale (CLCSS) | 1 year with one measurements points |
Status | Clinical Trial | Phase | |
---|---|---|---|
Active, not recruiting |
NCT05777044 -
The Effect of Hatha Yoga on Mental Health
|
N/A | |
Recruiting |
NCT04680611 -
Severe Asthma, MepolizumaB and Affect: SAMBA Study
|
||
Recruiting |
NCT04977232 -
Adjunctive Game Intervention for Anhedonia in MDD Patients
|
N/A | |
Recruiting |
NCT04043052 -
Mobile Technologies and Post-stroke Depression
|
N/A | |
Completed |
NCT04512768 -
Treating Comorbid Insomnia in Transdiagnostic Internet-Delivered Cognitive Behaviour Therapy
|
N/A | |
Recruiting |
NCT03207828 -
Testing Interventions for Patients With Fibromyalgia and Depression
|
N/A | |
Completed |
NCT04617015 -
Defining and Treating Depression-related Asthma
|
Early Phase 1 | |
Recruiting |
NCT06011681 -
The Rapid Diagnosis of MCI and Depression in Patients Ages 60 and Over
|
||
Completed |
NCT04476446 -
An Expanded Access Protocol for Esketamine Treatment in Participants With Treatment Resistant Depression (TRD) Who do Not Have Other Treatment Alternatives
|
Phase 3 | |
Recruiting |
NCT02783430 -
Evaluation of the Initial Prescription of Ketamine and Milnacipran in Depression in Patients With a Progressive Disease
|
Phase 2/Phase 3 | |
Recruiting |
NCT05563805 -
Exploring Virtual Reality Adventure Training Exergaming
|
N/A | |
Completed |
NCT04598165 -
Mobile WACh NEO: Mobile Solutions for Neonatal Health and Maternal Support
|
N/A | |
Completed |
NCT03457714 -
Guided Internet Delivered Cognitive-Behaviour Therapy for Persons With Spinal Cord Injury: A Feasibility Trial
|
||
Recruiting |
NCT05956912 -
Implementing Group Metacognitive Therapy in Cardiac Rehabilitation Services (PATHWAY-Beacons)
|
||
Completed |
NCT05588622 -
Meru Health Program for Cancer Patients With Depression and Anxiety
|
N/A | |
Recruiting |
NCT05234476 -
Behavioral Activation Plus Savoring for University Students
|
N/A | |
Active, not recruiting |
NCT05006976 -
A Naturalistic Trial of Nudging Clinicians in the Norwegian Sickness Absence Clinic. The NSAC Nudge Study
|
N/A | |
Enrolling by invitation |
NCT03276585 -
Night in Japan Home Sleep Monitoring Study
|
||
Completed |
NCT03167372 -
Pilot Comparison of N-of-1 Trials of Light Therapy
|
N/A | |
Terminated |
NCT03275571 -
HIV, Computerized Depression Therapy & Cognition
|
N/A |