None listed
Conditions
Interventions
Intervention1: Integrated Demonstration Program: Experimental arm will be assessed for knowledge by pretest on day 0. Experimental arm will also be assessed for competency on day 0. Intervention is g
Sponsors
Tata Memorial Hospital,
Eligibility
Inclusion criteria
Inclusion criteria: 1.Nursing staff working in TMH and ACTREC 2.Those who are temporary and permanent 3.Nurses who have educational qualification of GNM, B.Sc. / Diploma in Oncology Nursing/ M.Sc. Nursing
Exclusion criteria
Exclusion criteria: 1.Nurses who have problems with dexterity due to CNS involvement 2.Who have problems with eyesight for cannulation 3.Nursing staff with biohazard precautions such as HIV, Hepatitis B 4.Staff who have not taken vaccination against Hepatitis
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To find out the level of knowledge on intravenous cannulation therapy in terms of prevention of chemotherapy related intravenous complications in control and experimental group of pre and post integrated demonstration program among nursing staff.Timepoint: at day 7 and day 30 after completing integrated demonstrated program on day 0 | — |
Secondary
| Measure | Time frame |
|---|---|
| association between demographic data and competency skills on intravenous cannulation in terms of prevention of chemotherapy related intravenous complicationsTimepoint: at day 30 after completing integrated demonstrated program on day 0;association between demographic data and knowledge in terms of prevention of chemotherapy related intravenous complicationsTimepoint: at day 30 after completing integrated demonstrated program on day 0;prevention of chemotherapy related intravenous complicationsTimepoint: at day 7 and day 30 after completing integrated demonstrated program on day 0 | — |
Countries
India
Contacts
Public ContactMrs Prathepa Jagdish
Tata Memorial Hospital, Parel, Mumbai-12
Outcome results
None listed