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Core-Based Movement and Nutritional Counselling for Stress and Metabolic Outcomes in Overweight Women With Functional Constipation

StatusRecruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗
Trial flagged as At Risk
Primary endpoints removed 3 → 1 primary endpoints
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Record History

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  1. Recruitment opened Show 5 more changesShow less
    • Start date changed from estimate of Aug 25, 2026 to Oct 4, 2026
    • Eligibility criteria expanded, about 13 words
    • Secondary endpoints: details revised at 4 of 5 entries
    • Study description expanded, about 7 words
    • Site details revised
  2. Primary endpoint(s) modified
    • Secondary endpoints: 3 to 5
    v3
  3. Secondary endpoints: details revised at 3 of 3 entries
    • Eligibility criteria shortened, about 2 words
    v2
  4. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
Cairo University
1,562 trials monitored
See 18 trials at risk
This study will investigate the effect of core-based movement and nutritional counselling on stress, serum cortisol, and lipid profile in overweight women with functional constipation. Sixty overweight women with functional constipation will be randomly assigned into two equal groups. The study group will include 30 participants who will receive a core-based movement exercise program for 8 weeks, two sessions per week, in addition to guideline-based nutritional counselling. The control group will include 30 participants who will receive guideline-based nutritional counselling only for 8 weeks. The outcomes will include perceived stress, serum cortisol level, lipid profile, stool form, sleep quality, and quality of life.
Trial Details
NCT Number NCT07694830
Lead Sponsor Cairo University
Conditions
(from sponsor)		 Functional Constipation
Enrollment 60 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov