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Trial registered on ANZCTR
Registration number
ACTRN12615000167561
Ethics application status
Approved
Date submitted
8/02/2015
Date registered
20/02/2015
Date last updated
11/10/2018
Type of registration
Retrospectively registered
Titles & IDs
Public title
Efficacy of a physical activity program and typical advice about physical activity in cancer cachexia patients
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Scientific title
The efficacy of physical activity program and typical advice about physical activity in improving the physical activity in cancer cachexia patients.
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Secondary ID [1]
286129
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NIL
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Universal Trial Number (UTN)
U1111-1167-0458
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Cancer Cachexia
294135
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Cancer, Lung-Non small cell
294193
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Cancer, Lung Small cell
294194
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Condition category
Condition code
Cancer
294453
294453
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0
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Lung - Non small cell
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Cancer
294454
294454
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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
The participants were included in exercise program had two session exercise per week for 12 weeks and supervised by expert physiotherapists. the program was tailored to the individual patient's level of physical activity. Program include Aerobic exercise, resistance exercise and flexibility exercise. All the program was done under direct supervision of physiotherapist. Exercise was done for two minutes at each station (6 stations), with a minute intermission/pause when the patient lifted to the later stationand duration of the exercise each session about 30 miutes including the warming-up whcih before starting the 6 stations.. The exercises were involved resistance exercise as standing push-up, chest and shoulders, step up , flexible exercise such as shoulder stretch and aerobic exercise. Aerobic exercise include walking for 10-20 minutes of an intensity of 40%-70% of predicted heart maximum rates or 8-13 on the 15-point Borg's scale for rating of perceived of exertion..Centre for Epidemiologic Studies Depression Scale (CES-D) Questionnaires, EuroQoL Group EQ-5D-5L Questionnaires for quality of life was used. Short Physical performance Battery test, Six-Minute Walk test where used.
All this intervention done under direct supervision pf expert physiotherapist with more than 10 years experience.
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Intervention code [1]
291125
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Lifestyle
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Intervention code [2]
291126
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Rehabilitation
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Comparator / control treatment
Control group will not receive any intervention program.
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Control group
Active
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Outcomes
Primary outcome [1]
294240
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To determine the effects of an exercise program, compared with the usual care on the QoL (Quality of life) in cancer cachexia patients with underlying stage IV NSCLC.
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Assessment method [1]
294240
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Timepoint [1]
294240
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4, 8 and 12 weeks
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Primary outcome [2]
294295
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The effect of exercise program compared with the usual care on physical performance in cancer cachexia patients with underlying stage IV NSCLC
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Assessment method [2]
294295
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Timepoint [2]
294295
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Data will be collected at base line after 4 weeks from intervention, for both control and intervention group.
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Secondary outcome [1]
312972
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To study the effects of an exercise program compared with usual care on depression in the participants by questionnaire Centre for Epidemiologic Studies Depression Scale (CES-D-20).
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Assessment method [1]
312972
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Timepoint [1]
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12 weeks from baseline
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Eligibility
Key inclusion criteria
Inclusion criteria was patients with cancer cachexia with a confirmed diagnosis of late-stage NSCLC.
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Minimum age
25
Years
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Maximum age
70
Years
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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
Patients who have the same type of cancer but do not have cancer cachexia.
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Study design
Purpose of the study
Educational / counselling / training
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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Masking / blinding
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Who is / are masked / blinded?
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Intervention assignment
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Other design features
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Phase
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Type of endpoint/s
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Statistical methods / analysis
Interim analysis is to be conducted following the 1st 30 participants.
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Recruitment
Recruitment status
Stopped early
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Data analysis
Data collected is being analysed
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Reason for early stopping/withdrawal
Lack of funding/staff/facilities
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Date of first participant enrolment
Anticipated
5/02/2015
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Actual
5/02/2015
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Date of last participant enrolment
Anticipated
14/12/2017
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Actual
10/04/2015
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Date of last data collection
Anticipated
25/12/2017
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Actual
15/10/2015
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Sample size
Target
286
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Accrual to date
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Final
30
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Recruitment outside Australia
Country [1]
6638
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Egypt
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State/province [1]
6638
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Cairo
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Funding & Sponsors
Funding source category [1]
290704
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University
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Name [1]
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National Cancer Institute
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Address [1]
290704
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National Cancer Institute
Fom El Khalid, Cairo 11796, Egypt
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Country [1]
290704
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Egypt
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Primary sponsor type
University
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Name
National Cancer Institute
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Address
National Cancer Institute
Fom El Khalid, Cairo 11796, Egypt
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Country
Egypt
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Secondary sponsor category [1]
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None
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Name [1]
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No more secondary sponsor
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Address [1]
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It was the primary sponsor
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Country [1]
289396
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
294369
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Institutional Review Board Decision
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Ethics committee address [1]
294369
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National Cancer Institute, Cairo University, Egypt.
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Ethics committee country [1]
294369
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Egypt
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Date submitted for ethics approval [1]
294369
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20/11/2014
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Approval date [1]
294369
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25/11/2014
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Ethics approval number [1]
294369
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201516009.7
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Ethics committee name [2]
294370
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National Cancer Institute
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Ethics committee address [2]
294370
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National Cancer Institute, Cairo University,Fom El Khalig, Cairo, Egypt, 11796.
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Ethics committee country [2]
294370
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Egypt
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Date submitted for ethics approval [2]
294370
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Approval date [2]
294370
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25/11/2014
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Ethics approval number [2]
294370
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MD2010014012.3, IRB No IRB00004025, FWA No RWA00007284
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Summary
Brief summary
A prospective two-armed randomised, controlled (RCT) pilot study was conducted on 30 participants (15 cases and 15 controls) to check the effects of a physical exercise program (12 weeks) compared to usual care on physical performance and quality of life in cancer cachexia patients with underlying stage IV non-small cell lung cancer.
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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
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Prof Wafa Taha
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Address
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National Cancer Institute
Fom El Khalid, Cairo 11796, Egypt
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Country
54746
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Egypt
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Phone
54746
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+201222168097
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Fax
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Email
54746
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[email protected]
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Contact person for public queries
Name
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Prof Wafa Taha
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Address
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Fom El Khalid Cairo 11796 National Cancer Institute, Cairo
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Country
54747
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Egypt
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Phone
54747
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+201222168097
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Fax
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Email
54747
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[email protected]
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Contact person for scientific queries
Name
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Wafa Taha
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Address
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National Cancer Institute
Fom El Khalid, Cairo 11796, Egypt
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Country
54748
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Egypt
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Phone
54748
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+201222168097
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Fax
54748
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Email
54748
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[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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