Effects of Mobilization and Caffeine After Cesarean

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18-35
SponsorKTO Karatay University

About this trial

This study Maims to assess bowel motility, pain and psychological well-being in women in the post-cesarean period by mobilizing them early and encouraging them to consume coffee.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Being between 18 and 35 years of age,

Women who underwent cesarean delivery under spinal anesthesia,

Having a post-cesarean pain level of 4 or higher,

Being able to understand and write Turkish and communicate effectively with researchers.

Disqualifiers

Women who underwent emergency cesarean delivery,

Those with pregnancy complications (preeclampsia, placenta previa, etc.),

Those with a history of chronic gastrointestinal disease (e.g., irritable bowel syndrome, Crohn's disease, ulcerative colitis),

Those with sensitivity or allergy to caffeine,

Trial design

Design model

Parallel

Treatments tested in this trial

  • caffeine consumption

    Dietary supplement

    The women in the intervention group will be mobilised at the 4-hour mark. The intervention group will be given caffeinated Turkish coffee at 6-hour intervals.

  • Decaffeinated coffee

    Dietary supplement

    The women in the control group will be mobilised at the 6-hour mark. The control group will be given decaffeinated Turkish coffee at 6-hour intervals.

Treatment groups

60 Participants
are divided into 2 treatment groups
Group A: Control GroupPlacebo comparator 1 intervention
Group B: intervention groupExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Change in postoperative pain after caesarean section within 24 hours from baseline

Pain will be assessed using a 10 cm visual analogue scale. '0' means no pain, while '10' means unbearable pain. The assessment will be carried out at the start of the study, at 6-hour intervals, and at the end.

Time frame
Starting point, after intervention at 6 hours, 12 hours, 18 hours and 24 hours
2

Change in postoperative Bowel Motility after caesarean section within 24 hours from baseline

Bowel motility will be assessed using BFI. The Bowel Function Index (BFI) is a short and practical measure used to assess constipation, particularly in patients using opioids. It consists of three questions, each scored on a scale of 0 to 100. These scores are used to measure the degree of bowel dysfunction.

Time frame
Starting point, after intervention at 6 hours, 12 hours, 18 hours and 24 hours
3

Change in postoperative Psychological Well-being after caesarean section within 24 hours from baseline

Psychological Well-being will be assessed using Psychological Well-Being Scale. Based on the score obtained: 1.00-2.99 → Low psychological resilience, 3.00-4.30 → Moderate level, 4.31-5.00 → High psychological resilience.

Time frame
Starting point, after intervention at 6 hours, 12 hours, 18 hours and 24 hours

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.