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CompletedNCT01546233Updated Jul 6, 2016

Multidisciplinary Education in Lung Cancer Patients Who Receiving Chemotherapy Treatment

An observational study in Lung Cancer, sponsored by Department of Medical Services Ministry of Public Health of Thailand. Completed at 1 site in Thailand. Open to participants aged 45 Years to 65 Years. Per ClinicalTrials.gov, last updated 2016-07-06.

Sponsored by Department of Medical Services Ministry of Public Health of Thailand · Observational

Study type
Observational
Model
Case-control
Time perspective
Cross-sectional
Enrollment
60
Ages
45 Years to 65 Years
Sex
All
01

Study summary

The purpose of this study is to compare the fatigue in lung cancer patients receiving chemotherapy treatment, between the education programme in self-care a multidisciplinary with the group who received standard care.

Read the detailed description

Educate of self-care by Oncology nurses to relieve and prevent the fatigue of cancer chemotherapy, and provide the manual to read at home, take about 15 minutes. By using home exercise program, 30 minutes of physical education. Teaching and demonstration exercises of the muscles to breath and conservation of energy during exercise and record the exercise/walking diary, the nutritional education nutrition counseling, psychiatric assessment,self-care prevention of depression.

02

Conditions studied

  • Lung Cancer

Keywords

  • Lung cancer
  • Chemotherapy
  • Multidisciplinary self care programme
  • Fatigue
03

In context

Lung Neoplasms

7,333 studies on the registry are indexed under Lung Neoplasms; 1,554 are open to participants now.

This study's enrollment of 60 is below the median of 190 across 1,547 observational studies indexed under Lung Neoplasms.

Browse Lung Neoplasms studies →

Lead sponsor

Department of Medical Services Ministry of Public Health of Thailand is the lead sponsor of 39 studies on the registry; 10 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
45 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Fatigue Lung Cancer Patients

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  1. Aged 45-65 years.
  2. Has been diagnosed lung cancer stages 3-4 must be chemotherapy is platinum-based, and had received chemotherapy for at least one time, must be in the range of 2-4 cycles of chemotherapy.
  3. Performance status: ECOG 0-1
  4. No problem hearing it.
  5. Read and write Thai.
  6. Be willing to cooperate in research. And signed a joint research

Exclusion criteria

Exclusion Criteria:

  1. The complications include: high fever, severe nausea and vomiting.
  2. Injection drug use in diabetes treatment.
  3. Ischemic heart disease with heart arrhythmia and the drug continuously.
  4. Is unable to daily living. Caused by defects in movement, and severe osteoarthritis, muscle atrophy, paralysis or walking flat less than 10 meters.
05

Study design

Observational model
Case-control
Time perspective
Cross-sectional
Enrollment
60 participants (actual)

Groups and cohorts

  • multidisiplinary self care program

    Patient with Lung cancer will be participated in group education with multidisiplinary self care program

    Behavioral: multidisciplinary education programme

  • Conventional education

    Lung cancer patient will be received standard education

    Behavioral: standard education

Interventions

  • Behavioralmultidisciplinary education programme

    Educate of self-care by Oncology nurses to relieve and prevent the fatigue of cancer chemotherapy, and provide the manual to read at home, take about 15 minutes. By using home exercise program, 30 minutes of physical education. Teaching and demonstration exercises of the muscles to breath and conservation of energy during exercise and record the exercise/walking diary, the nutritional education nutrition counseling, psychiatric assessment,self-care prevention of depression.

    Also known as: multidisciplinary self care education programm

  • Behavioralstandard education

    standard education before and after chemotherapy

    Also known as: standard education before and after chemotherapy

06

What researchers measure

Primary outcomes

  1. Measure fatigue by questionnaires

    Time frame: August 2011 to august 2012 (up to 1 year)

07

Study locations

1 site
  • Department of Chemotherapy Unit, Rajavithi Hospital
    Bangkok, Bangkok 10400, Thailand
08

References and documents

Individual participant data

Plan to share: Yes — ๋Journal of the medical association of Thailand

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
Not marked actual or estimatedDates not marked actual or estimated

The record gives a start of Mar 2012, a primary completion of Sep 2012 and a completion of Dec 2012. It does not say whether these dates are actual or estimated.

How these figures are worked out, and which studies are left out of them.

Registered
Mar 1, 2012
First posted
Mar 7, 2012
Start
Mar 2012
Primary completionActual
Sep 2012
CompletionActual
Dec 2012
Last update
Jul 6, 2016
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Jul 6, 2016, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT01546233
Lead sponsor
Department of Medical Services Ministry of Public Health of Thailand
Responsible party
Sponsor
First posted
Mar 7, 2012
Start date
Mar 2012
Primary completion
Sep 2012
Completion
Dec 2012
Last update
Jul 6, 2016

Study contacts

Kotchukorn Wnagnum, Msc (nurse)
principal investigator · Department of Medical Services Ministry of Public Health of Thailand

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Mar 2012. You cannot join it, but the record below documents what was studied.

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