TCTR20220802001CompletedPhase 2
the effectiveness of An Integrated Symptom related Fatigue Management Program (ISFMP) on pain, anxiety, fatigue score and lactate levels in low risk pregnant woman during childbirth.
Faculty of Nursing0 sites65 target enrollmentStarted: August 2, 2022Last updated:
Conditions
Trial Snapshot
- Phase
- Phase 2
- Status
- Completed
- Sponsor
- Enrollment
- 65
Study Overview
Brief Summary
The participants in the comparison and experimental groups had varying pain, anxiety, fatigue scores and lactate levels throughout the progression of labor. Pain, anxiety, and fatigue in the experimental group were statistical significantly lower than the comparison group. There were no statistical significantly difference in lactate level between two groups.
Study Design
- Study Type
- Interventional
Eligibility Criteria
- Ages
- 18 Years to 34 Years (—)
- Sex
- Female
Inclusion Criteria
- •Inclusion criteria were; 18 to 35 years of age; 32-34 weeks gestational age and receiving care at the antepartum clinic until 37-41+6 weeks of pregnancy; understanding of the Thai language; admission to the labour unit in the active phase; possession and ability to use their smart phone and deliver their newborns at the study hospital. Exclusion criteria, at the antenatal clinic were: 1) high anxiety score (> 70); high fatigue score (>70); high lactate level (> 4)
Exclusion Criteria
- •Exclusion criteria in the labor room were; high-risk pregnancy; instrumental vaginal delivery; and C/S or delivery complication. The 80 subjects were grouped into 40 matched pairs. Each pair was matched on fatigue score at baseline and age.
Investigators
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