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Effect of a Nursing Teaching Protocol on Mastitis Prognosis: Quasi-Experimental Research Design

A

Assiut University

Status

Completed

Conditions

Mastitis

Treatments

Other: Mastitis care teaching protocol

Study type

Interventional

Funder types

Other

Identifiers

NCT05974956
Mastitis prognosis

Details and patient eligibility

About

Aim: Evaluate the effect of a nursing teaching protocol on mastitis prognosis. Research design: Quasi-experimental research design was utilized. A convenient sample of sixty adult female patients diagnosed with mastitis, Patients divided equally into two groups(study and control) thirty for each.

Full description

The study was conducted in the breast unit in general surgery department at Main Assiut University Hospital. A convenient sample of sixty adult female patients diagnosed with mastitis, their ages range from 20 to 65years old. Patients divided equally into two groups; thirty for each. Both groups had been assessed at base line using the following tools:

Tool (I): An interview questionnaire sheet Tool (II):Mastitis self-care practices Tool (III): Numeric pain rating scale Tool (IV): Mastitis prognosis sheet

The control group exposed to routine care and study group received mastitis teaching protocol. After three weeks; both groups had been reassessed by the same tools.

Data analysis had been performed by using the Statistical Package for the Social Sciences (SPSS) Categorical variables described by number and percent (N, %). Continuous variables described by mean and standard deviation (Mean, SD). Chi-square test and Fisher exact test used to compare between categorical variables .T-test and Pearson's chi-square used to appear the association between patients' knowledge, practice, and mastitis prognosis before implementation of nursing teaching protocol and three weeks post.

Enrollment

60 patients

Sex

Female

Ages

20 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Exclusion Criteria:

  1. Mental health problems
  2. Visual or hearing problems
  3. Uncooperative

Trial design

Primary purpose

Prevention

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

60 participants in 2 patient groups

Control group
No Intervention group
Description:
The control group exposed to routine care.
Study group
Experimental group
Description:
The study group received the sessions of "mastitis care teaching protocol".
Treatment:
Other: Mastitis care teaching protocol

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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