Home Telemonitoring for Patients With Lung Cancer

Lung Cancer Clinical Trial

— HTPLC  

Official title:

PILOT: Home Telemonitoring for Self-Management Education of Patients With Lung Ca

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01670539
• Other study ID #: H-22930
• Secondary ID: 1R15CA150999
• Status: Completed
• Phase: N/A
• Start date: April 2011
• Est. completion date: June 2013

Study information

• Verified date: December 2021
• Source: West Virginia University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to learn more about using a home machine "Telemonitor" to find problems people with lung cancer may have after being discharged from the hospital and help them manage problems by contacting their healthcare provider.The study hypothesis is that patients with lung CA using short-term (14 days)home telemonitors, educated/coached by nurses on telemonitor data risks/implications for the first two weeks after hospital discharge, will be able to self-report their signs/ symptoms to the clinician resulting in decreased use of costly health care resources over 60 days.

Description:

All patients in the study will receive usual care after hospital discharge. This study also involves an interview and review of your medical records, and uses the "telemonitor" machine to measure your temperature, pulse, oxygen level,weight and blood pressure. The telemonitor will also ask you to press YES or NO buttons in response to questions on your symptoms such as difficulty breathing. Research nurses will come to your home 3 times and it will take about 30 minutes for each visit for the nurse to record the information using the telemonitor. You will also be asked to fill out a survey about your ability to do activities and your health status. This will take approximately another 30 minutes. You may or may not receive the small telemonitor (about as big as a large book) for 14 days after discharge to provide additional information to the researchers. If you receive the monitor for the full 14 days, you or someone you ask us to train will be taught to use the monitor every morning to collect information on how you will "talk" to you to tell you to put a blood pressure cuff on your arm and an oxygen measurer on your finger. You will step on a scale to take your weight and you will use a forehead sensor to take your temperature. The blood pressure, weight, temperature, your pulse, and your oxygen level will be recorded by the monitor. It will then ask you at least 10 questions and you will push a yes or no button indicating how much difficulty you are having with your daily activities and shortness of breath. The monitor will then connect to your telephone line using a no-charge "800" number and transmit the information to the researchers. If you do not have a phone, a special antenna will be connected to the monitor to transmit the information wirelessly. The nurse will call you every day for the 14 days when you have the monitor. If you do not receive the monitor for the full 14 days, you will still have the monitor used by the nurse when you are visited at least 3 times at home to gather information on how you are doing after hospital discharge. These home monitor visits will be within 2 days after discharge, 2 weeks after discharge, and 2 months after discharge. The main difference is that the monitor will not be left in your home but will be brought by the nurse on each visit. You will also receive a phone call to ask you questions about the study at 1 month after discharge. If you do not have a phone, you will receive another home visit. Whether or not you get the monitor for the full 14 days will be determined randomly by computer before the nurse visits you at home the first time. are doing. The monitor will turn on each day at the same time; the monitor

Recruitment information / eligibility

• Status: Completed
• Enrollment: 47
• Est. completion date: June 2013
• Est. primary completion date: December 2012
• Accepts healthy volunteers: No
• Gender: All
• Age group: 45 Years to 90 Years

Eligibility

Inclusion Criteria:

(1) patients admitted to the hospital for lung CA as a primary or secondary diagnosis; (2) at least 45 years of age and up to 90 years old; (3) stable mental status and ability to speak (but not necessarily read) the primary language of the region (English).

Exclusion Criteria:

1. are not discharged to home settings

2. are discharged to hospice

3. display a verbalized inability to understand or answer the questionnaires, (4) are disqualified at the discretion of the treating physician, and/or (4) live beyond a 75 mile radius of the hospital.

Related Conditions & MeSH terms

• Lung Cancer
• Lung Neoplasms

Intervention

Device:
• HomMed Telemonitor
A "HomMed Telemonitor" wireless telemonitoring system collects data on a daily basis, including heart rate, blood pressure, oxygen level, body temperature, weight, responses to 9 pre-programmed questions (including difficulty breathing, fatigue, limited activities, difficulty taking meds, pain). Telemonitored results are transmitted to the research office for analysis and contact to patient by clinical research nurses.

Locations

Country	Name	City	State
United States	WVU Mary Babb Randolph Cancer Center and Ruby Hospital	Morgantown	West Virginia

Sponsors (2)

Lead Sponsor	Collaborator
West Virginia University	National Cancer Institute (NCI)

Country where clinical trial is conducted

United States, 

References & Publications (3)

Chen YJ, Narsavage GL, Culp SL, Weaver TE. The development and psychometric analysis of the short-form Pulmonary Functional Status Scale (PFSS-11). Res Nurs Health. 2010 Dec;33(6):477-85. doi: 10.1002/nur.20403. Epub 2010 Oct 18. — View Citation

Narsavage G, Romeo E. Education and support needs of younger and older cancer survivors. Appl Nurs Res. 2003 May;16(2):103-9. — View Citation

Narsavage GL, Naylor MD. Factors associated with referral of elderly individuals with cardiac and pulmonary disorders for home care services following hospital discharge. J Gerontol Nurs. 2000 May;26(5):14-20. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Changes in Telemonitor Data From Baseline: Temperature	Changes in temperature measured by telemonitor daily over 14 days after hospital discharge	14 days
Primary	Changes in Telemonitor Data From Baseline: Pulse Rate	Changes in pulse rate measured by telemonitor daily over 14 days after hospital discharge	14 days
Primary	Changes in Telemonitor Data From Baseline: Blood Pressure	Changes in blood pressure measured by telemonitor daily over 14 days after hospital discharge	14 days
Primary	Changes in Telemonitor Data From Baseline: SpO2	Changes in SpO2 measured by telemonitor daily over 14 days after hospital discharge	14 days
Primary	Changes in Telemonitor Data From Baseline: Weight	Changes in weight measured by telemonitor daily over 14 days after hospital discharge	14 days
Secondary	Changes in Telemonitor Symptoms Recorded From Baseline: Dyspnea	Numeric rating for dyspnea, from 0 to 10 with a lower number being a decrease in dysnea. Symptom data requiring yes-no answers to whether the symptom is worse today than yesterday : dyspnea are collected daily via telemonitor for 14 days.	14 days
Secondary	Changes in Telemonitor Symptoms Recorded From Baseline: Functioning	Pulmonary Functional Status Scale (PFSS-11) , scoring from 0 to 10 with increasing scores indicating an improvement in functioning. Symptom data requiring yes-no answers to whether the symptom is worse today than yesterday : general functioning activities, are collected daily via telemonitor for 14 days.	14 days
Secondary	Changes in Telemonitor Symptoms Recorded From Baseline: Pain	Numeric rating for pain (0 to 10 scale) with a lower number indicating less pain. Symptom data requiring yes-no answers to whether the symptom is worse today than yesterday : pain are collected daily via telemonitor for 14 days.	14 days