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Jacobson's Progressive Muscle Relaxation Technique on Children With Leukemia Undergoing Chemotherapy.

The Effect of Jacobson's Progressive Muscle Relaxation Technique on Anxiety and Fatigue Among Children With Leukemia Undergoing Chemotherapy.

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06631196
Acronym
JPMRT
Enrollment
80
Registered
2024-10-08
Start date
2024-11-01
Completion date
2025-11-30
Last updated
2024-10-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anxiety, Children, Fatigue Related to Cancer Treatment, Leukemia

Keywords

Jacobson's Progressive Muscle Relaxation Technique, Anxiety, Fatigue, Children, Leukemia, Chemotherapy, nursing care

Brief summary

The goal of this clinical trial is to determine the effect of Jacobson's progressive muscle relaxation technique on anxiety and fatigue among children with leukemia undergoing chemotherapy. The main research hypotheses are; * Children with leukemia who receive Jacobson's progressive muscle relaxation technique exhibit less anxiety than those who don't receive it. * Children with leukemia who receive Jacobson's progressive muscle relaxation technique exhibit less fatigue than those who don't receive it. Researchers will compare Jacobson's progressive muscle relaxation technique with standardized nursing care on a child's anxiety and fatigue.

Interventions

PROCEDUREJacobson's PMRT

each child in the intervention group will perform five sessions of Jacobson's PMRT. Each session lasted for 15-20 minutes under the supervision of the researcher.

Sponsors

Alexandria University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
7 Years to 15 Years
Healthy volunteers
Yes

Inclusion criteria

* Children diagnosed with leukemia and received chemotherapy sessions. * Age ranged from 7 to 15 years.

Exclusion criteria

* other disorders such as neurological diseases, cerebrovascular accidents, or mental illness.

Design outcomes

Primary

MeasureTime frameDescription
Pediatric Quality of Life Inventory (PedsQL) Multidimensional Fatigue Scale:before and after intervention.This tool was developed initially by (Smets et al., 1995) to assess fatigue for the subject. The scale comprised 18 items and 3 subscales which are; General Fatigue, Sleep/Rest Fatigue, and Cognitive Fatigue. The format, instructions, Likert response scale, and scoring method are identical to the PedsQL 4.0 Generic Core Scales, with higher scores indicating a better health-related quality of life (lower fatigue symptoms). A five-point Likert scale was used to evaluate the responses in which (zero= never a problem; one = almost never a problem; two= sometimes a problem; three= often a problem; four= almost always a problem). Items are reverse-scored and linearly transformed to a 0-100 scale as follows: * 0 = 100-76 * 1 = 75-51 * 2 = 50-26 * 3 = 25-1 * 4= 0

Secondary

MeasureTime frameDescription
Spence Children's Anxiety Scale - Child (SCAS-Child)before and after intervention.This tool was developed initially by Spence, S.H., (1997) to assess the severity of anxiety symptoms for the subject. The scale consists of six subscales: Separation Anxiety, Social Phobia, Obsessive Compulsive Problems, Panic/Agoraphobia, Generalized Anxiety/Overanxious Symptoms and Fears of Physical Injury. Scores consist of a total raw score (range from 0 to 114) and six sub-scale scores, with higher scores indicating greater severity of anxiety symptoms. Sub-scales are computed by summing the following items: * Separation anxiety (items 5, 8, 12, 15, 16, 44) * Social phobia (items 6, 7, 9, 10, 29, 35) * Obsessive-compulsive (items 14, 19, 27, 40, 41, 42) * Panic/agoraphobia (items 13, 21, 28, 30, 32, 34, 36, 37, 39) * Physical Injury (items 2, 18, 23, 25, 33) * Generalized anxiety (items 1, 3, 4, 20, 22, 24) Items that are not scored in either the total score or the sub-scale scores are 11, 17, 26, 31, 38, 43, 45, and 46. They are not scored because they did

Other

MeasureTime frameDescription
Socio Demographic and Medical Data of Children with leukemia Undergoing Chemotherapy Structured Interview Schedulebefore interventionThis tool will be developed by the researcher to assess the socio-demographic and medical data of children undergoing chemotherapy. It will include 2 parts: Part I: Socio-demographic data: It includes age, gender, educational level, and residence. Part II: Medical data of children: It includes onset of disease, type of leukemia, prescribed chemotherapy

Contacts

Primary ContactEman Badr, Phds
eman.badr@alexu.edu.eg01002347927

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026