Effects of Holistic Program for Reducing Fatigue among Sepsis Survivors

Phase 3

• Conditions: Sepsis Survivors; Holistic Program; Fatigue

• Registration Number: TCTR20240329002
• Lead Sponsor: /A

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2024-03-29
• Study Completion: 2024-07-31
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Pending (Not yet recruiting)
• Sex: All
• Target Recruitment: 68

Inclusion Criteria

1. Patient aged 18 - 85 years who treated sepsis for more than 48 hours with normal vital signs and no signs and symptoms associated with SIRS criteria and no symptoms and signs of multiple organ dysfunction according to SOFA or qSOFA criteria.
2. The patient has no physical abnormalities. (with bone injuries and arthritis, osteoarthritis, gout, etc.)
3. Patient aged 60 years and over after taking the Mini Cog test and receiving a score greater than or equal to 3 again.
4. Patient who has experience symptoms of fatigue, evaluated by using the Piper Fatigue Scale-12 questionnaire, moderate or higher or with a PFS-12 score greater than equal to 4 points.
5. Able to communicate by speaking, reading, and writing Thai.
6. The patient or caregiver has a smart phone. and can use the LINE application.

Exclusion Criteria

1. The patient has co-morbidities that cause fatigue easily which does not occur after sepsis, such as cancer undergoing chemotherapy or radiotherapy, HIV patients with a CD4 level lower than 350 cubic millimeters, chronic obstructive pulmonary disease, asthma, kidney failure stage 4 or higher, liver disease with Child Pugh Score C, anemia with hemoglobin less than 7 g/dl, malnutrition with serum albumin less than 2, heart failure. Have had a history of being infected with coronavirus 19, which was accompanied by fatigue.
2. Patients with neurological and brain disorders, such as spinal cord injuries, or had surgery related to the nervous system and brain.
3. Patients diagnosed with psychiatric disorders such as schizophrenia, bipolar disorder or severe depression.
4. Terminally ill patients or bedridden patients

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Fatigue severity score at baseline, 2 weeks after intervention and 4 weeks after intervention Piper Fatigue Scale 12

Secondary Outcome Measures

Name	Time	Method
/A N/A N/A