Efficacy of Seated Exercise on Functional Capacity and Quality of Life in Patients With Leukemia During Chemotherapy Cycles

Sponsor
Suez University
Study ID
NCT07740174
Status
Not Yet Recruiting

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Conditions

Eligibility Criteria

Sex
MALE
Age
30 Years - 40 Years
Healthy Volunteers
Not accepted

Interventions

  • Seated exercise — BEHAVIORAL
    Participants in the intervention group will perform a structured seated exercise program during their chemotherapy cycles. The exercise program will consist of supervised, individualized seated exercises designed to improve functional capacity and quality of life. The exercise sessions will be performed according to the study protocol throughout the intervention period. Each session will consist of a five-minute warm up, 20 minutes of moderate intensity repetitive motion exercises, and a five -minute cool-down. Functional outcomes will be assessed before and after the exercise program. including maximum voluntary ventilation , six-minute walk test distance, and FACT- G quesionnaire.

Study Details

This study aims to evaluate the efficacy of seated exercise on functional capacity and quality of life in patients with leukemia during chemotherapy cycles Participants will receive efficacy of seated exercise on functional capacity and quality of life in patients with leukemia during chemotherapy cycles over a defined period. Outcomes will be assessed using Pulmonary function test, 6 min walk test and FACT- G questionnaire to determine improvements in quality of life in cancer patient rehabilitation special to diagnosed with leukemia.

Key Dates

First listed
Jul 31, 2026
Start date
Aug 1, 2026
Status verified
Aug 2026
Primary completion
Nov 1, 2026
Completion
Dec 1, 2026

Study Design

Enrollment
30 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Arms

  • Experimental: Seated exercise group
  • No Intervention: control group
    control group will receive usual care/ standard advices

Primary Outcome Measure

change in functional capacity [ Time Frame: Baseline and after 4 weeks of intervention ]

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