Cancer Patients Clinical Trial
Official title:
Effectiveness of Video Assisted Self Management Program on Chemotherapy Side Effects in Terms of Knowledge, Self Efficacy and Severity of Side Effects Among the Cancer Patient Receiving Chemotherapy at Oncology Day Care
Verified date | March 2021 |
Source | Institute of Liver and Biliary Sciences, India |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
A study to assess the effectiveness of video assisted Self Management Program on chemotherapy side effects in terms of Knowledge, Self Efficacy and Severity of side effects among the Cancer patient receiving chemotherapy at Oncology day care ILBS , New Delhi. Primary Objective: 1. To assess the Knowledge, Self Efficacy and Severity of side effects of chemotherapy related side effects in the Experiment Vs. Comparison group among the cancer patients receiving chemotherapy. 2. To compare the knowledge and self efficacy scores in Experimental Vs. Comparison group after video assisted SMP among the cancer patients receiving chemotherapy. 3. To compare the severity of chemotherapy related side effects in Experiment Vs. Comparison group before and after video assisted SMP among the cancer patients receiving chemotherapy. Secondary Objective To find the correlation between knowledge and self efficacy scores among the cancer patients receiving chemotherapy under Experimental Group. 2. To determine the association of Severity of side effects with the knowledge and self efficacy scores among the cancer patients receiving chemotherapy. 3. To determine the association of knowledge, self efficacy with the socio demographic and clinical variables among the cancer patients receiving chemotherapy. The study assumes that: 1. Video assisted teaching is an accepted teaching strategy and enhances teaching learning activities. 2. Patients may have limited knowledge about the management of side effects related to chemotherapy including nausea, vomiting, diarrhea, Constipation, dry skin, fever, alopecia related distress and pain. 3. Patients may have decrease severity of chemotherapy related side effects including nausea, vomiting, diarrhea, Constipation , dry skin, fever , alopecia related distress and pain. After the self management program.
Status | Completed |
Enrollment | 60 |
Est. completion date | December 5, 2021 |
Est. primary completion date | November 14, 2021 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 65 Years |
Eligibility | Inclusion Criteria: All the cancer patients receiving chemotherapy at Onco day care ILBS which will be included in the study who- - Were 18 years or older - Patients who have undergone at least one chemotherapy cycle. - Patients who are stable. - Can Communicate in English / Hindi - Patients who are Mentally alert Exclusion Criteria: All cancer patients undergoing chemotherapy was excluded from the study who - - Patients who are Android mobile users Patients with visual and hearing impairments - Had hemodynamic instability. |
Country | Name | City | State |
---|---|---|---|
India | Institute of Liver and Biliary Sciences | New Delhi |
Lead Sponsor | Collaborator |
---|---|
Institute of Liver and Biliary Sciences, India |
India,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Knowledge regarding the management of chemotherapy related side effects. | A structured 20 item knowledge questionnaire developed for assessment of knowledge among the cancer patients receiving chemotherapy at Onco day care Ilbs. The knowledge questionnaire will be self reported by the subjects. | up to 5 weeks | |
Primary | self efficacy in relation to symptom management relevant to chemotherapy for patients with cancer. | The Structured Symptom-Management Self-Efficacy Scale derived from - Symptom-Management Self-Efficacy Scale Breast Cancer (SMSES-Breast Ca.) It was developed by SY Liang et al., in 2015 that measure perceived self efficacy in terms of respondent's ability to self manage the symptoms of chemotherapy. It is an 11-point Likert scale was used for each item that ranged from 0 (not confident at all) to 10 (completely confident), with higher scores representing higher perceived self-efficacy. | up to 5 weeks | |
Primary | Severity of Side effects including Nausea, Vomiting, Diarrhea, Constipation, Mucositis, Fever, Pain ,Dry Skin and alopecia related distress. | It consists of grades which are used to assess the severity of adverse events. Grades ranges from 0 to 5. The scores assessed by the researcher for the severity of side effects will be verified by the doctors on duty.
The Distress thermometer was developed as a simple tool to effectively screen for symptom of Alopecia related distress. It is a self reported tool using a 0-10 rating scale. The scale was explained to all the participants and participants were asked to circle or pick a number 0-10 from the drop down box that best describes how much distress patient have been experiencing in the past weeks including today. |
up to 5 weeks |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT03707548 -
BPT to Improve Bodily Disturbances in Post-treatment Cancer Patients
|
N/A | |
Not yet recruiting |
NCT06463782 -
Clinical Study of 68Ga-LNC1007 Injection PET/CT
|
Phase 1 | |
Not yet recruiting |
NCT04493450 -
NEMO - an App for Side Effect Management in Oncology
|
||
Completed |
NCT05604820 -
The Effect of Progressive Muscle Relaxation Exercise on Sleep Quality
|
N/A | |
Completed |
NCT04024748 -
Verification of Imaging System PCD-1000A
|
||
Completed |
NCT03320161 -
A Patient Consensus for the Research in Supportive Care in French Cancer Care Centers: the CyPRES Project
|
||
Recruiting |
NCT05547282 -
Low-dose Radiotherapy Combined With Conventional Radiotherapy After Immunotherapy Failure
|
N/A | |
Recruiting |
NCT01742143 -
Impact of ICCAN on Cancer Treatment Completion and Quality of Life
|
||
Recruiting |
NCT01603316 -
Food: A Three-Arm Study Examining Food Insecurity Interventions
|
Phase 2 | |
Recruiting |
NCT03100071 -
Central Venous Catheter (CVC) Associated Deep Vein Thrombosis (DVT) in Cancer Patients
|
||
Completed |
NCT04037410 -
Environmental Temperature and White Adipose Tissue in Cancer Patients
|
||
Recruiting |
NCT06305741 -
A Study of an Anxiety Intervention for Latino/Latina/Hispanic Older Adults With Cancer and Their Caregivers
|
N/A | |
Recruiting |
NCT05279378 -
Correlation of Lung Ultrasonography With Chest CT Findings in Cancer Patients With COVID-19 Viral Pneumonia
|
||
Completed |
NCT03536702 -
Effect of Group Led Creative Writing on Mood in Cancer Patients
|
N/A | |
Not yet recruiting |
NCT05922423 -
Exploration of Management Model and Intervention Research on Fear of Cancer Recurrence
|
N/A | |
Completed |
NCT01704469 -
A Comparison of the Perception of a Needle Injection Pain Between Cancer Patients Receiving Opioid Therapy Versus Opioid-naive Patients
|
N/A | |
Active, not recruiting |
NCT06348940 -
Effects of Behavioral Activation on Negative Emotions, Cancer-related Symptoms and Clinical Indicators in Cancer Patients
|
N/A | |
Completed |
NCT04302792 -
New Food Solutions for Cancer Patients
|
N/A | |
Recruiting |
NCT05219851 -
The Risk Factors for Acute Radiation Pneumonitis in Patients With Prior Receipt of Immune Checkpoint Inhibitors
|
||
Completed |
NCT05884047 -
The Effect Of Virtual Reality Glasses On Vital Signs And State Anxiety Level In Cancer Patients
|
N/A |