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The Effect of Relaxation Program on Coping With Stress and Anxiety Levels of Caregivers of Children With Cancer.

G

Gazi University

Status

Not yet enrolling

Conditions

Caregivers With a Child Followed up With a Cancer Diagnosis

Treatments

Other: Relaxation Program

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

This research will be carried out to determine the effect of the relaxation program applied to the caregivers of children followed by the diagnosis of cancer on the levels of caregivers' anxiety and coping with stress. The research will be conducted in a single-blind parallel-group randomized controlled trial design. A relaxation program including progressive muscle relaxation exercises will be applied to caregivers. The application will be carried out by sending muscle relaxation videos and videos for relaxation to mothers. The relaxation program is planned to last approximately 6 weeks

Full description

In this study, a relaxation program will be applied to mothers who have a child followed up with a cancer diagnosis. The relaxation program will include progressive muscle relaxation exercises and videos for relaxation. Initial applications will be implemented with caregivers. The relaxation program is planned to last 6 weeks. The program is planned to last 8 weeks in total, with pre-test and post-test applications. Caregivers will then be asked to perform the treatments each week. Coping with Stress and State-Trait Anxiety Scale will be used at the beginning and end of the program.

Enrollment

50 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion criteria

  • The child has received cancer treatment for at least two months,
  • Those who have internet access on their smartphone or computer
  • Those who can continue the work for six weeks (doing progressive relaxation exercises at least 2 times a week)

Exclusion Criteria:

  • Those whose children/caregivers are in the terminal period,
  • Those whose child/caregiver has not received chemotherapy treatment,
  • Those who take medication for anxiety or use one of the complementary medicine approaches.

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

50 participants in 2 patient groups

Intervention
Experimental group
Description:
caregivers receiving a relaxation program
Treatment:
Other: Relaxation Program
Control group
No Intervention group
Description:
the group that did not receive any training

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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