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Quality of life and FOCUS program intervention in acute leukemia patients and their family caregivers

Quality of life and FOCUS program intervention in acute leukemia patients and their family caregivers

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300070442
Enrollment
Unknown
Registered
2023-04-12
Start date
2023-05-01
Completion date
Unknown
Last updated
2023-06-04

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

Conditions

Acute Leukemia (AL)

Interventions

Group 1:FOCUS program
A cross-sectional descriptive study group:N/A

Sponsors

The Second Affiliated Hospital of Air Force Medical University/School of Nursing, Air Force Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Inclusion criteria for current study patients: (1) Diagnostic criteria refer to WHO 2016 Classification criteria for hematopoietic and lymphoid tumors; (2) Aged >=18 years; (3) The patient has no mental disorder, clear consciousness and normal communication ability; (4) The patient needs family caregivers in daily life; (5) Patients gave informed consent to this study and voluntarily participated in the investigation. 2. Randomized controlled trial patient inclusion criteria: (1) Diagnostic criteria refer to WHO 2016 Classification criteria for hematopoietic and lymphoid tumors; (2) Aged >=18 years; (3) The patient has no mental disorder, clear consciousness and normal communication ability; (4) The patient needs family caregivers in daily life; (5) Patients gave informed consent to the study and voluntarily participated in the investigation; (6) Trait coping style scores tend to be negative coping. 3. Inclusion criteria of primary caregivers in the family: (1) Aged >=18 years; (2) The primary caregiver designated by the patient; (3) The family members who live with the patient should take care of the patient for at least 4 hours a day; (4) To provide patients with living care and medical care, can make decisions and assume the main responsibility for patients' clinical treatment; (5) No history of mental disorders or cancer, no cognitive or communication disorders; (6) Informed consent and voluntary participation in this study. 4. Inclusion criteria for primary caregivers in randomized controlled trials: (1) Aged >=18 years; (2) The primary caregiver designated by the patient; (3) The family members who live with the patient should take care of the patient for at least 4 hours a day; (4) To provide patients with living care and medical care, can make decisions and assume the main responsibility for patients' clinical treatment; (5) No history of mental disorders or cancer, no cognitive or communication disorders; (6) Informed consent and voluntary participation in this study.

Exclusion criteria

Exclusion criteria: 1. Exclusion criteria for patients in current study: (1) Patients with mental disorders, cognitive disorders or visual and hearing disorders who are unable to communicate normally; (2) Serious physical diseases accompanied by other systems; (3) Patients live alone or live with nannies, nursing workers, etc.; (4) Participate in other studies during the investigation period and have a significant impact on this study; (5) Patients who are not willing to cooperate or have poor compliance. 2. Exclusion criteria for patients in randomized controlled trials: (1) Patients with mental disorders, cognitive disorders or visual and hearing disorders who are unable to communicate normally; (2) Serious physical diseases accompanied by other systems; (3) Patients live alone or live with nannies, nursing workers, etc.; (4) Patients who have undergone other intervention studies; (5) Patients who are not willing to cooperate or have poor compliance. 3. Exclusion criteria for primary caregivers in the family: (1) Serious impairment of physical health and complicated with other major diseases; (2) Emotional instability due to other stressful events recently; (3) Cognitive communication disorder, unable to carry out normal language communication; (4) Termination of care responsibilities for other reasons; (5) Unwilling to participate in this study. 4. Exclusion criteria for primary caregivers in randomized controlled trials: (1) Serious impairment of physical health and complicated with other major diseases; (2) Emotional instability due to other stressful events recently; (3) Cognitive communication disorder, unable to carry out normal language communication; (4) Discontinuation of care duties for other reasons; (5) Unwilling to participate in this study.

Design outcomes

Primary

MeasureTime frame
The Quality of Life;

Secondary

MeasureTime frame
Familily Resilience;Cognitive Appraisal;Coping Strategies;

Countries

China

Contacts

Public ContactLiu Li

The Second Affiliated Hospital of Air Force Medical University

liuli1@medmail.com.cn+86 13488222789

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026