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DEFINITIONS
Trial Review
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Trial registered on ANZCTR
Registration number
ACTRN12613000342718
Ethics application status
Not yet submitted
Date submitted
25/02/2013
Date registered
27/03/2013
Date last updated
27/03/2013
Type of registration
Prospectively registered
Titles & IDs
Public title
Lung INterdisciplinary Clinic (LINC): reducing biopsychosocial distress in patients with lung cancer and mesothelioma
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Scientific title
The effectiveness of an outpatient interdisciplinary team in reducing biopsychosocial distress in patients with lung cancer and mesothelioma
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Secondary ID [1]
282020
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None
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Universal Trial Number (UTN)
U1111-1139-8500
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Trial acronym
LINC
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Lung Cancer
288466
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Mesothelioma
288467
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Condition category
Condition code
Cancer
288812
288812
0
0
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Lung - Mesothelioma
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Cancer
288813
288813
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0
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Lung - Non small cell
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Cancer
288814
288814
0
0
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Lung - Small cell
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Participants attend an initial 1/2 hour session with an allied health professional for an assessment using the Distress Thermometer. This involves an assessment of the participant's overall distress and the problems which may be contributing to their distress. Following completion of this assessment the following interventions/referrals, described below, will be completed.
PRACTICAL PROBLEMS:
* Child care:
Social Worker (SW): Referral to Cancer Council practical support program, assistance to apply for child care rebate.
* Housing:
SW: Information & assistance with emergency accommodation, temporary accommodation for rural patients during treatment, applications to Homeswest & Residential Care
Occupational Therapist (OT): Equipment & home modifications
* Insurance/Financial:
SW: Assistance & advocacy in accessing income protection insurance, superannuation benefits, Centrelink payments, financial aid & referral to financial counselors
* Transportation:
SW: Referral to transport services for assistance, assistance with Australian Council for Rehabilitation Of the Disabled (ACROD)/Taxi User Subsidy Scheme (TUSS) applications
* Work/school:
SW: Liaison & advocacy with workplace/school e.g. coordinating medical certificates from the doctor, liaising with school counselors/chaplains for children.
* Treatment decisions:
Cancer Nurse Coordinator (CNC): Ensure patient & family are aware of all treatment options (including no treatment), provide written information & ensure adequate understanding of it, provide strategies to make a decision, refer to counseling services, inform & communicate with the treating team.
FAMILY PROBLEMS:
* Dealing with children:
SW: Counseling & support regarding communicating with children, referral to counseling services for children, assessing carer stress & providing practical assistance to young carers, child protection.
* Dealing with partner:
SW: Counseling & support regarding communicating with partner, referral to counseling services (e.g. Cancer Council, Western Australian Psycho-Oncology Service (WAPOS), Silver Chain Hospice Service (SCHS), referral to domestic violence services if applicable, assessing carer stress & providing practical assistance to partners/carers
* Ability to have children:
CNC: Identify if the treatment will affect fertility & provide information regarding the impact on fertility, refer to reproductive endocrinologist, inform treating team which may include delaying treatment.
* Family health issues:
CNC: Identify what the health issues are, refer appropriately
SW: Counseling & support to cope with this stress, inform/refer to practical services to assist the family member, referral to counseling services.
EMOTIONAL PROBLEMS:
* All problem items:
SW: Counseling & support, risk assessment of self harm, referral to counseling services, liaison with General Practitioner (GP)/treating doctor (in the case of mental health background/symptoms), liaison with existing community supports (e.g. psychiatrist, psychologist, chaplain, school counselor etc) & information regarding Solaris Centre.
SPIRITUAL/RELIGIOUS CONCERNS:
* ALL: Referral to spiritual services at Sir Charles Gairdner Hospital (SCGH) or linking in with own community spiritual group
PHYSICAL PROBLEMS:
* Appearance:
ALL: Referral to Look Good…Feel Better
SW: Counseling & support & referral to counseling services.
* Bathing/dressing:
SW: Referral to support services for assistance at home
OT: Provision of adaptive equipment such as shower chair or long handled sponge, referral for OT home visit to assess for rails or home modification, education on energy conservation strategies.
* Breathing:
SW: If anxiety related; counseling & support, referral to psychology services.
OT: Education on controlled breathing and/or relaxation exercises.
Physiotherapist (PT): Assessment of titration requirement of medically prescribed oxygen for physical activity & education of non pharmacological interventions in management of breathlessness, coughing & airway clearance.
* Changes in Urination:
PT: Assessment & management of continence in collaboration with Continence Management Team.
CNC: assess if related to disease or treatment. Refer back to treating team if required.
* Constipation:
CNC: assess cause of constipation, discuss some simple medication options and natural dietary options.
* Diarrhoea:
CNC: assess cause and give advice as appropriate.
* Eating:
Dietition (DT): Assessment of nutritional needs, nutritional status and diet. Provision of education and counseling for recommended foods/food preparation methods to achieve nutritional needs; management of nutrition-related side effects of treatment; access to nutritional supplements
* Fatigue:
OT: Education on energy conservation strategies, provision of adaptive equipment, referral for OT home visit, education on strategies to improve sleep.
PT: Exercise advice & prescription.
* Feeling Swollen:
OT: Upper limb lymphoedema management.
CNC: assess cause and liaise with medical team
* Fevers:
CNC: assess cause and direct patient to appropriate follow up (Accident and Emergency if greater than 38 degrees celcius and having treatment)
* Getting Around:
OT: Provision of equipment such as a shower chair, referral for OT home visit.
PT: Assessment of physical capacity to identify impairment, exercise advice & prescription, mobility assessment, education regarding optimising safe mobilisation & mobility aid prescription.
* Indigestion:
CNC: assess cause (medications, diet, treatments, other) discuss with appropriate team members.
* Memory/Concentration:
OT: Formal assessment of cognition, education on compensatory strategies to cope with cognitive changes, referral to outside services such as Memory Clinic, or Day Hospital OT, referral for OT home visit to look at appropriate set-up of home environment to promote safety.
* Mouth Sores:
CNC: assess cause and if on treatment. May need to see GP
* Nausea:
CNC: assess cause. Refer appropriately to treatment team (or appropriate nurses-radation oncology/medical oncology) or discuss medication regime for antiemetics and educate about how to improve symptoms.
* Nose dry/congested:
CNC: assess cause and discuss with appropriate team members
* Pain:
PT: Assessment & non pharmacological treatment interventions in appropriate cases.
CNC: assess pain, discuss with appropriate team members (treating doctors, GP, Silver Chain Hospice or Palliative Care Service), educate regarding current pain medications
* Sexual:
SW: Counseling & support, referral to specialist counseling services, referral to Menopause Clinic at King Edward Memorial Hospital (KEMH), liaison with GP/treating doctors
* Skin Dry/Itchy:
CNC: assess cause and discuss with appropriate team members. Simple skin care advice and education offered
* Sleep:
OT: Education on sleep hygiene strategies and appropriate set-up of sleep environment, provision of pressure relieving devices to increase comfort in lying.
* Substance abuse:
SW: Assessment of use & motivation for change, referral to rehabilitation services.
* Tingling in Hands/Feet:
OT: Provision of adaptive equipment.
OTHER PROBLEMS:
* Falls/Near Falls:
OT: Education on falls prevention, provision of adaptive equipment, referral for OT home visit to assess falls risks in the home.
PT: Exercise advice & prescription, mobility assessment regarding optimising safe mobilisation, falls prevention & mobility aid prescription.
* Discomfort in Sitting/Lying:
OT: Provision of appropriate pressure relieving devices and positioning advice.
PT: Assessment of discomfort & treatment interventions in appropriate cases.
* Driving:
SW: Referral to transport services.
OT: Referral for OT driving assessment for patients with a condition which may impair their ability to drive.
* Smoking:
OT: Advice and education regarding quitting smoking.
* Medications:
ALL: Information regarding webster packs & referral back to the medical team.
SW: Referral to medication prompt services.
* Completing household chores:
SW: Referral for in home support services.
OT: Advice regarding adaptive equipment
* Legal:
SW: Information regarding legal documents (including Will, Enduring Power of Attorney (EPA) Enduring Power of Guardianship (EPG), Advanced Health Directive (AHD), low cost legal services & Guardianship & Administration applications. Liaison & advocacy with the justice or immigration systems.
* Lack of information regarding diagnosis, treatment or follow up plan:
CNC: provide information on disease, staging or treatment as appropriate for patient. Ensure rural patients have options for treatment closer to home as appropriate. Educate and support patient throughout disease (progression or recurrence) as to treatment plan and aim.
* Weight Loss:
DT: Assessment of nutritional needs, nutritional status and diet. Provision of education and counseling for recommended foods/food preparation methods to achieve nutritional needs; management of nutrition-related side effects of treatment; access to nutritional supplements
Following the completion of all the required interventions for the participant (this will vary for each participant), a follow up Distress Thermometer with problem checklist and qualitative questionnaire will be completed within 1-7 days via telephone. Should participants have future conerns they will have access to he allied health team for the duration of the research (April 2013 - September 2013).
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Intervention code [1]
286603
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Early detection / Screening
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Intervention code [2]
286604
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Rehabilitation
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Intervention code [3]
286810
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Lifestyle
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Comparator / control treatment
No control group
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
288955
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Reduction in Distress and number of concerns, measured on the Distress Thermometer and problem checklist, of >1 point
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Assessment method [1]
288955
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Timepoint [1]
288955
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A Baseline Distress Thermometer with problem checklist will be completed at initial contact. Following completion of all allied health interventions, as directed by the treating clinician, a repeat Distress Thermometer with problem checklist will be completed via phone between 1 and 7 days. For example the allied health intervention may include the fabrication of a custom made cushion for increasing comfort in sitting and improved positioning. The treating Occupational Therapist may complete this intervention within 1 hour with a follow up call in 3 days. Following the follow up call if no modifications are required, the Occupational Therapist will close the intervention for this participant. The repeat Distress Thermometer will occur 1-7 days post the closure of this participant's intervention. Should a participant recieve interventions from more than 1 health professional, follow up will occur following the completion of the last health professional to complete their intervention.
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Secondary outcome [1]
301433
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Satisfaction questionairre
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Assessment method [1]
301433
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Timepoint [1]
301433
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Following completion of all allied health interventions, as directed by the treating clinician, a qualitative questionnaire to determine the participant's experience of the clinic will be completed via phone between 1 and 7 days. For example the allied health intervention may include the fabrication of a custom made cushion for increasing comfort in sitting and improved positioning. The treating Occupational Therapist may complete this intervention within 1 hour with a follow up call in 3 days. Following the follow up call if no modifications are required, the Occupational Therapist will close the intervention for this participant. The repeat Distress Thermometer will occur 1-7 days post the closure of this participant's intervention. Should a participant recieve interventions from more than 1 health professional, follow up will occur following the completion of the last health professional to complete their intervention.
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Eligibility
Key inclusion criteria
All patients with lung cancer or mesiothelioma who are under the care of any/all medical oncologist, respiratory physician, radiation therapist, palliative care specialist at Sir Charles Gairdner Hospital
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Minimum age
18
Years
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Maximum age
No limit
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
under 18 years of age, cognitive impairment, non-English speaking
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Non-randomised trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Potential participants will be identified as follows:
1. All new lung cancer patients discussed at the weekly Multidisciplinary Lung Cancer meeting will be invited to participate via letter and phone call.
2. All existing lung cancer patients can be referred by any clinical staff member.
3. Posters will be placed in the outpatient clinics and participants can self refer.
The lead investigator will provide eligible participants with the patient information sheet and explanation of all aspects of the research. The participants will be provided with a written copy of the consent form and will be requested to read the information sheet and consent form. Time to discuss participation with their next of kin/guardian will be provided.
No concealment procedures required as all receive assessment and treatment
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
No randomisation
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Masking / blinding
Open (masking not used)
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Who is / are masked / blinded?
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Intervention assignment
Single group
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Other design features
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Phase
Not Applicable
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Type of endpoint/s
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Statistical methods / analysis
Comparisons between pre and post test will be made using standard analyses such as paired t-tests and linear mixed models. Demographic variables such as participants age, gender, living situation, participants diagnosis, years since diagnosis, stage of disease, current functional analysis via an Australian Modified Karnovky Performance Scale (AMKPS) will be considered as confounders.
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Recruitment
Recruitment status
Not yet recruiting
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Date of first participant enrolment
Anticipated
1/04/2013
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Actual
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Date of last participant enrolment
Anticipated
30/09/2013
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Actual
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
150
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
WA
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Recruitment hospital [1]
680
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Sir Charles Gairdner Hospital - Nedlands
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Recruitment postcode(s) [1]
6427
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6009 - Nedlands
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Funding & Sponsors
Funding source category [1]
286802
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Hospital
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Name [1]
286802
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Sir Charles Gairdner Hospital
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Address [1]
286802
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Hospital Avenue, Nedlands WA 6009
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Country [1]
286802
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Australia
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Primary sponsor type
Hospital
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Name
Sir Charles Gairdner Hospital
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Address
Hospital Avenue, Nedlands WA 6009
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Country
Australia
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Secondary sponsor category [1]
285594
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Other Collaborative groups
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Name [1]
285594
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Cancer and Palliative Research Evaluation Unit (CaPCREU)
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Address [1]
285594
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School of Surgery M507, UWA, 35 Stirling HWY, Crawley WA 6009
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Country [1]
285594
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Australia
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Ethics approval
Ethics application status
Not yet submitted
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Ethics committee name [1]
288870
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Sir Charles Gairdner and Osbourne Park Group.
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Ethics committee address [1]
288870
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Hospital Avenue, Nedlands WA 6009
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Ethics committee country [1]
288870
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Date submitted for ethics approval [1]
288870
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26/02/2013
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Approval date [1]
288870
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Ethics approval number [1]
288870
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2012-207
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Summary
Brief summary
This study will attempt to determine what causes distress in lung cancer and mesothelioma patients and whether having access to an interdisciplinary team reduces this distress. Who is it for? You may be eligible to join this study if you are 18 years or over with lung cancer or mesothelioma, and currently under the care of any/all medical oncologist, respiratory physician, radiation therapist, palliative care specialist at Sir Charles Gairdner Hospital. Trial details: Participants in this trial will receive access to allied health staff (including Social worker, Physiotherapist, Occupational Therapist, Dietitian and Clinical Nurse) who can assist them with strategies for reducing or managing their concerns. The overall duration of this study will be 6 months in which we will aim to assess all patients with a new diagnosis of lung cancer or mesothelioma and existing patients as required. Study aims: To compare distress in lung cancer and mesothelioma patients before and after having access to a team of allied health staff to address their concerns.
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
38122
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Mrs Kellie Blyth
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Address
38122
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Occupational Therapy Department, Sir Charles Gairdner Hospital, Hospital Avenue, Nedlands WA 6009
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Country
38122
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Australia
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Phone
38122
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+610893462855
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Fax
38122
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+610893463599
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Email
38122
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[email protected]
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Contact person for public queries
Name
38123
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Kellie Blyth
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Address
38123
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Occupational Therapy Department, Sir Charles Gairdner Hospital, Hospital Avenue, Nedlands WA 6009
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Country
38123
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Australia
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Phone
38123
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+610893462855
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Fax
38123
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+610893463599
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Email
38123
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[email protected]
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Contact person for scientific queries
Name
38124
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Kellie Blyth
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Address
38124
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Occupational Therapy Department, Sir Charles Gairdner Hospital, Hospital Avenue, Nedlands WA 6009
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Country
38124
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Australia
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Phone
38124
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+610893462855
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Fax
38124
0
+610893463599
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Email
38124
0
[email protected]
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No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
No additional documents have been identified.
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