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Improving Oral Care to Reduce Mouth Problems in Children Receiving Chemotherapy

Development and Implementation of an Evidence-Based Oral Care Bundle to Reduce the incidence and severity of Oral Mucositis among children with cancer Receiving Chemotherapy - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/09/094222
Enrollment
80
Registered
2025-09-04
Start date
Unknown
Completion date
Unknown
Last updated
2025-09-15

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

Conditions

Health Condition 1: C910- Acute lymphoblastic leukemia [ALL] Health Condition 2: C402- Malignant neoplasm of long bones of lower limb Health Condition 3: C810- Nodular lymphocyte predominant Hodgkin lymphoma Health Condition 4: C920- Acute myeloblastic leukemia Health Condition 5: C717- Malignant neoplasm of brain stem Health Condition 6: C692- Malignant neoplasm of retina

Interventions

Intervention1: oral care bundle: The intervention consists of a structured oral care bundle including regular oral hygiene with fluoride toothpaste, cryotherapy (popsicles), application of honey, and

Sponsors

Malabar Cancer Centre Post Graduate Institute of Oncology Sciences and Research
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Children aged 1 to 14 years diagnosed with cancer. Children receiving chemotherapy agents known to carry a high risk of causing oral mucositis as inpatients. Children who can be monitored for mucositis for up to 14 days after receiving chemotherapy. Parents or caregivers who give informed consent.

Exclusion criteria

Exclusion criteria: ?Children with congenital anomalies or other severe comorbidities that may interfere with oral care assessments. ?Children who have initiated their chemotherapy regimen in other units or hospitals, outside the study setting.

Design outcomes

Primary

MeasureTime frame
Reduce the incidence and severity of Oral Mucositis among children Receiving ChemotherapyTimepoint: Day 1 to day 14 of chemotherapy

Secondary

MeasureTime frame
Change in nursing knowledge score (pre-test,post-test)Timepoint: Immediately pre-training and immediately post-training;percentage of children maintaining adequate oral intake during 1?14 Days of chemoTimepoint: post-implementation (Day 1?14 of chemo cycles);Caregiver satisfaction scoreTimepoint: Post-implementation - during discharge;Caregiver adherence rate to bundle tasksTimepoint: Daily during hospitalization;Nurse satisfaction score with bundle implementationTimepoint: At 1 month post-implementation (and optionally at 3 and 6 months);Nurse adherence rate to bundleTimepoint: Weekly during implementation period

Countries

India

Contacts

Public ContactAnjana G N

Malabar Cancer Centre - Post Graduate Institute of Oncology Sciences and Research

anjuanjanagn@gmail.com9497641912

Outcome results

None listed

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