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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04292678
Other study ID # N/Y
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date April 1, 2020
Est. completion date July 1, 2021

Study information

Verified date March 2020
Source Hacettepe University
Contact Merve Gulbahar, RN,Res.Assis
Phone +90312 305 15 80/181
Email gulbaharmerve@hotmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Caregivers of patients with advanced cancer will be entered. Participants will be randomized to one of two study arms: Arm 1: Progressive muscle relaxation; Arm 2: Attention matched control. Hypothesis: Progressive muscle relaxation will decrease caregiving burden and severity of fatigue and improve quality of life.


Description:

Previous reports have revealed that progressive muscle relaxation to use to decrease symptom burden associated with cancer. However, there have been limited studies that directly focus on supporting caregivers of advanced cancer patients who face serious problems in diagnosis and treatment process, at least as much as cancer patients. Besides, till date, no study has been conducted to determine the effects of progressive relaxation exercise on caregiver burden, fatigue and quality of life in those providing care for patients with advanced cancer. The present study investigates the effects of progressive muscle relaxation in a single-site, 2-arm, randomized, controlled study of 64 caregivers of patients with advanced cancer. Arm 1: relaxation; Arm 2: Attention matched control. The investigators hypothesize that progressive muscle relaxation will decrease severity of caregiver burden and fatigue and improve quality of life.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 64
Est. completion date July 1, 2021
Est. primary completion date April 30, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- Literate

- Providing care for advanced cancer patients (stage III-IV) for at least 6 months

- Primary caregiver (caring for the longest time)

- No communication problem

- Not using any other non-pharmacological approach during the study period

Exclusion Criteria:

- Providing care for individuals with early-stage (Stage I-II) cancer

- Caregivers who providing care services for a fee

- Having a history of psychiatric disorder (major depression, etc.)

- Not willing to participate in the study

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Progressive muscle relaxation
The progressive muscle relaxation intervention will last for 20 minutes and comprise sessions involving tensing and relaxing the body with deep breathing. The participants will perform progressive muscle relaxation for each body part in order, starting with the facial muscles and head, followed by neck, shoulders, chest, abdomen, legs, and feet; all muscle tension and relaxation procedures were performed accompanied with deep breathing. The participants will be instructed to tense a specified group of muscles for 5 s and relax it for 10 s while breathing out. Throughout this exercise, the participants will visualize a wave of relaxation flowing over their body using the deep-breathing technique.
Other:
Attention matched control
Caregivers of patients with advanced cancer will receive only a training group session about general cancer information such as risk factors, treatment methods, and treatment-related side effects, lasting 20 minutes first week of the study.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Hacettepe University

Outcome

Type Measure Description Time frame Safety issue
Primary Change in caregiver burden severity Caregiver burden severity will be measured based on patient report by Experience-Based Caregiver Burden Scale in Advanced Cancer.
Maximum scores indicate worse caregiver burden.
Baseline measurements, at the end of 8th week and two weeks after the completion of the interventions
Primary Change in fatigue severity Fatigue severity will be measured based on patient report by the Fatigue Severity Scale. Minimum scores indicate better level of fatigue. Baseline measurements, at the end of 8th week and two weeks after the completion of the interventions
Primary Change in Quality of life status Quality of life will be measured by the Caregiver's Quality of Life Index-Cancer Scale. Maximum scores indicate better quality of life. Baseline measurements, at the end of 8th week and two weeks after the completion of the interventions
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