Diese Seite wurde automatisch übersetzt und die Genauigkeit der Übersetzung wird nicht garantiert. Bitte wende dich an die englische Version für einen Quelltext.

Effects of a Soya-Based Fibre Beverage on Weight and Health in Overweight Adults (SBB-WEIGHTLOSS)

21. Mai 2026 aktualisiert von: Wan Rosli Wan Ishak, Universiti Sains Malaysia

Research on the Effect of Soya-Based Dietary Fibre Beverages (SBB) in Improving Anthropometric Parameters and Biomarker Profiles Among Overweight Students and Staff in Health Campus, Universiti Sains Malaysia, Kelantan

The goal of this intervention study is to evaluate the effect of soya-based dietary fiber beverage (SBB) in overweight adults. The main question it aims to answer is:

Does the SBB effective in improving the weight and metabolic parameters among overweight adults?

Overweight participants will be randomly assigned to intervention or control group for a defined intervention period. The intervention involved the consumption of the SBB beverage powder while allowing participants to maintain their usual meal portions. while the control group will be asked to continue their usual breakfast, lunch, and dinner meals during the study period. Clinical and biochemical parameters will be assessed at baseline and after the intervention period to evaluate potential metabolic changes. Anthropometric and body composition will be recorded. Assessments will include questionnaires related to food frequency (FFQ), food diary, physical activity (IPAQ), satiety and appetite, and defecation behavior.

Studienübersicht

Status

Abgeschlossen

Bedingungen

Intervention / Behandlung

Detaillierte Beschreibung

Dietary fiber plays a crucial role in weight management by enhancing satiety, reducing caloric intake, and modulating gut microbiota. Among various fiber sources, soya- based dietary fiber (SBB) is of particular interest due to its combined benefits of soluble and insoluble fiber, plant-based proteins, and bioactive compounds. Studies have shown that soya proteins and isoflavones contribute to lipid metabolism, insulin sensitivity, and overall weight reduction. However, there is limited research on the direct impact of soya-based dietary fiber beverages (SBB) on weight loss and metabolic health outcomes. In this study, the investigators have already developed soya-based dietary fiber beverage (SBB) formulated with soymilk powder, apple mixture powder, and botanical powder. While the formulation has been completed, its efficacy in improving anthropometric parameters and metabolic profiles among overweight adults remains untested. Individuals who agree to participate in this study will be divided into two groups: the Control Group and the Intervention Group. The intervention involves consume two servings of the beverage at least 30 min before each breakfast and teatime every day for 12 weeks, while the control group will be asked to continue their usual breakfast, lunch, and dinner meals during the study period. Regular consumption of the SBB beverage over three months may lead to significant improvements in metabolic health, including a reduction in body weight, improved body composition, and enhanced satiety response. Additionally, participants are expected to show positive changes in dietary intake patterns, physical activity levels, and quality of life. Biomarker analysis will further assess the impact of the intervention on metabolic and inflammatory parameters.

Studientyp

Interventionell

Einschreibung (Tatsächlich)

42

Phase

  • Unzutreffend

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienorte

  • Malaysia
    • Kelantan
      • Kubang Kerian, Kelantan, Malaysia, 16150
        • Health Campus, Universiti Sains Malaysia

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

  • Erwachsene

Akzeptiert gesunde Freiwillige

Ja

Beschreibung

Inclusion Criteria:

  • Staff or students aged 18-50 years
  • Participants with BMI 23-30 kg/m2
  • Participants physically inactive
  • Not having any allergies to any of the known food ingredients, especially milk and soy
  • Not on lipid-lowering and oral hypoglycemic drugs
  • No kidney diseases

Exclusion Criteria:

  • Pregnant or lactating mothers
  • Having known chronic disease conditions
  • Having a known allergy history for soy and milk or any of the ingredients in the formula.
  • History of any type of minor or major surgical procedure in the past 6 months.
  • Currently on diet prescriptions or participating in regular physical activity sessions.
  • On weight loss drugs or consuming dietary supplements such as protein shakes, whey protein, casein, fruit juices or fiber-based supplements.

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Behandlung
  • Zuteilung: Zufällig
  • Interventionsmodell: Parallele Zuordnung
  • Maskierung: Keine (Offenes Etikett)

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Experimental: Soya-based dietary fibre beverage
The SBB beverage was in powdered form (1 sachet contain 53g of powder), and participants were instructed to prepare the liquid shake by mixing the 1 sachet of the powder with 250 mL of cold water in a shaker that had been provided. They were asked to consume two servings of the beverage at least 30 min before each breakfast and teatime every day for 12 weeks. The intervention group was given a sufficiently SBB sachet with a label indicating the ingredients and the preparation method. The breakfast, lunch, and dinner meals were recommended as normal meals (the meals that they habitually eat). The intervention involved the consumption of the SBB beverage powder while allowing participants to maintain their usual meal portions. There was no strict portion control, and participants could continue their habitual eating patterns. The focus was on incorporating the SBB beverage as part of their daily diet without restricting overall food intake.
Nahrungsergänzungsmittel: Soya-based dietary fibre beverage
The intervention consume two servings of the beverage at least 30 min before each breakfast and teatime every day for 12 weeks. One serving is one sachet (53g) of beverage powder in 250 mL cold water. There was no strict portion control, and participants could continue their habitual eating patterns. The focus was on incorporating the SBB beverage as part of their daily diet without restricting overall food intake.
Kein Eingriff: Habitual diet
The control group was asked to continue their usual breakfast, lunch, and dinner meals during the study period

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Change in weight (kg)
Zeitfenster: Baseline, week 4, week 8 and week 12
Changes in body weight (kg) from baseline to week 12
Baseline, week 4, week 8 and week 12
Change in body fat percentage (%)
Zeitfenster: Baseline, week 4, week 8 and week 12
Change in body fat percentage (%) from baseline to week 12.
Baseline, week 4, week 8 and week 12
Change in body mass index (BMI) kg/m^2
Zeitfenster: Baseline, week 4, week 8 and week 12
Changes in BMI (kg/m^2) from baseline to week 12. Weight (kg) and height (m) will be measured and combined to report BMI in kg/m²
Baseline, week 4, week 8 and week 12
Change in waist circumference (cm)
Zeitfenster: Baseline, week 4, week 8 and week 12
Change in waist circumference (cm) from baseline to week 12
Baseline, week 4, week 8 and week 12
Change in hip circumference (cm)
Zeitfenster: Baseline, week 4, week 8 and week 12
Changes in hip circumference (cm) from baseline to week 12
Baseline, week 4, week 8 and week 12
Change in body fat mass (kg)
Zeitfenster: Baseline, week 4, week 8 and week 12
Change in body fat mass (kg) from baseline to week 12.
Baseline, week 4, week 8 and week 12
Change in body fat-free mass (kg)
Zeitfenster: Baseline, week 4, week 8 and week 12
Change in body fat-free mass (kg) from baseline to week 12.
Baseline, week 4, week 8 and week 12
Change in visceral fat rating
Zeitfenster: Baseline, week 4, week 8 and week 12
Change in visceral fat rating from baseline to week 12. Visceral Fat Rating from 1 to 12: Indicates a healthy level of visceral fat. Visceral Fat Rating from 13 to 59: Indicates an excess level of visceral fat.
Baseline, week 4, week 8 and week 12
Change in muscle mass (kg)
Zeitfenster: Baseline, week 4, week 8 and week 12
Change in muscle mass (kg) from baseline to week 12.
Baseline, week 4, week 8 and week 12

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Change in blood pressure (mmHg)
Zeitfenster: Baseline, week 4, week 8 and week 12
Change in systolic blood pressure (mmHg) and diastolic blood pressure (mmHg) from baseline to week 12.
Baseline, week 4, week 8 and week 12
Change in total cholesterol (mg/dL)
Zeitfenster: Baseline and week 12
Change in total cholesterol (mg/dL) from baseline to week 12
Baseline and week 12
Change in low-density lipoprotein (LDL) (mg/dL)
Zeitfenster: baseline and week 12
Change in low-density lipoprotein (LDL) (mg/dL) from baseline to week 12
baseline and week 12
Change in high-density lipoprotein (HDL) (mg/dL)
Zeitfenster: Baseline and week 12
Change in high-density lipoprotein (HDL) (mg/dL) from baseline to week 12
Baseline and week 12
Change in triglycerides (mg/dL)
Zeitfenster: Baseline and week 12
Change in triglycerides (mg/dL) from baseline to week 12
Baseline and week 12
Change in total protein (g/L)
Zeitfenster: Baseline and week 12
Change in total protein (g/L) from baseline to week 12
Baseline and week 12
Change in albumin (g/L)
Zeitfenster: Baseline and week 12
Change in albumin (g/L) from baseline to week 12
Baseline and week 12
Change in bilirubin (µmol/L)
Zeitfenster: Baseline and week 12
Change in bilirubin (µmol/L) from baseline to week 12
Baseline and week 12
Change in alkaline phosphatase (ALP) (U/L)
Zeitfenster: Baseline and week 12
Change in alkaline phosphatase (ALP) (U/L) from baseline to week 12
Baseline and week 12
Change in alanine transaminase (ALT) (U/L)
Zeitfenster: Baseline and week 12
Change in alanine transaminase (ALT) (U/L) from baseline to week 12
Baseline and week 12
Change in aspartate aminotransferase (AST) (U/L)
Zeitfenster: Baseline and week 12
Change in aspartate aminotransferase (AST) (U/L)
Baseline and week 12
Change in gamma-glutamyl transferase (GGT) (U/L)
Zeitfenster: Baseline and week 12
Change in gamma-glutamyl transferase (GGT) (U/L) from baseline to week 12
Baseline and week 12
Change in urea (mmol/L)
Zeitfenster: Baseline and week 12
Change in urea (mmol/L) from baseline to week 12
Baseline and week 12
Change in estimated Glomerular Filtration Rate (eGFR) (mL/min)
Zeitfenster: Baseline and week 12
Change in estimated Glomerular Filtration Rate (eGFR) (mL/min) from baseline to week 12
Baseline and week 12
Change in creatinine (µmol/L)
Zeitfenster: Baseline and week 12
Change in creatinine (µmol/L) from baseline to week 12
Baseline and week 12
Change in Interleukin-6 (IL-6) (pg/mL)
Zeitfenster: Baseline and week 12
Change in IL-6 (pg/mL) and C-reactive protein from baseline to week 12
Baseline and week 12
Change in C-reactive protein (mg/mL)
Zeitfenster: Baseline and week 12
Change in C-reactive protein (mg/mL) from baseline to week 12.
Baseline and week 12

Andere Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Physical activity level (MET-minutes/week)
Zeitfenster: Baseline and week 12
Physical activity was assessed using the Malay version of the International Physical Activity Questionnaire (IPAQ). The data was processed according to the official IPAQ scoring protocol. The results are reported as continuous scores expressed in Metabolic Equivalent of Task (MET)-minutes per week. Higher scores indicate a greater volume of physical activity expenditure.
Baseline and week 12
Change in Diet
Zeitfenster: Baseline, week 4 and week 12
Change in average daily diet intake, assessed using 24-hour recalls and 3-day food records. Dietary data were entered into Nutritionist Pro™ software (Axxya Systems, USA) to estimate mean daily energy and nutrient intake, including macronutrients and dietary fibre. For food items that are not available in the Malaysian Nutrient Composition of Foods, the USDA nutrient database was referred. For mixed dishes that were not available in the database, local recipes were entered into the software.
Baseline, week 4 and week 12
Change in appetite
Zeitfenster: Baseline, week 4 and week 12
Subjective appetite sensations were assessed using an eleven-point numerical rating scale (NRS), with anchors at 0 ("not at all") and 10 ("very much"), to evaluate hunger, fullness, desire to eat, thirst, and prospective food consumption. Participants completed the questionnaire before and after breakfast, lunch, and dinner at each study time point (pre, week 4, and post). For analysis and comparability with conventional visual analogue scale (VAS) methods, NRS scores were linearly transformed to a 0-100 scale by multiplying each value by 10.
Baseline, week 4 and week 12
Frequency of defecation
Zeitfenster: Baseline, week 4 and week 12
Frequency of defecation will be assessed using the Questionnaire of Regularity of Defecation Behavior. Participants will report the frequency of bowel movements categorized as 1 time/day, more than 1 time/day, 2-3 times/week, or 4-5 times/week.
Baseline, week 4 and week 12
Time of defecation
Zeitfenster: Baseline, week 4 and week 12
Time of defecation will be assessed using the Questionnaire of Regularity of Defecation Behavior. Participants will report the usual timing of bowel movements within specified time intervals over a 24-hour period.
Baseline, week 4 and week 12
Stool consistency
Zeitfenster: Baseline, week 4 and week 12
Stool consistency will be assessed using the Bristol Stool Form Scale, a 7-point scale ranging from Type 1 (hard lumps indicating constipation) to Type 7 (watery stool indicating diarrhea). Types 3 and 4 indicate normal stool consistency.
Baseline, week 4 and week 12
Stool color
Zeitfenster: Baseline, week 4 and week 12
Stool color will be assessed using the Questionnaire of Regularity of Defecation Behavior. Participants will report stool color categorized as brown, yellow, black, red, green, or blue.
Baseline, week 4 and week 12
Stool amount per defecation
Zeitfenster: Baseline, week 4 and week 12
Amount of stool per defecation will be assessed using the Questionnaire of Regularity of Defecation Behavior and categorized as 1-2 stools, 3-4 stools, or more than 5 stools.
Baseline, week 4 and week 12
Feces odor
Zeitfenster: Baseline, week 4 and week 12
Feces odor will be assessed using the Questionnaire of Regularity of Defecation Behavior and categorized as regular or irregular.
Baseline, week 4 and week 12
Ease of defecation
Zeitfenster: Baseline, week 4 and week 12
Ease of defecation will be assessed using the Questionnaire of Regularity of Defecation Behavior and categorized as easy or hard defecation.
Baseline, week 4 and week 12
Effect on quality of life
Zeitfenster: Baseline and week 12
The quality of life outcome will be assessed using the World Health Organization Quality of Life-BREF (WHOQOL-BREF) questionnaire, a 26-item instrument evaluating four domains: physical health, psychological health, social relationships, and environment. Each domain score ranges from 0 to 100, with higher scores indicating better quality of life. Assessments will be conducted at baseline (pre-intervention) and after completion of the intervention (post-intervention).
Baseline and week 12

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Sponsor

Universiti Sains Malaysia

Ermittler

  • Hauptermittler: Wan Rosli Wan Ishak, PhD, School of Health Sciences, Universiti Sains Malaysia, Health Campus, 16150 Kubang Kerian, Kelantan, Malaysia

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn (Tatsächlich)

30. Juni 2025

Primärer Abschluss (Tatsächlich)

1. Dezember 2025

Studienabschluss (Tatsächlich)

1. Dezember 2025

Studienanmeldedaten

Zuerst eingereicht

15. Mai 2026

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

21. Mai 2026

Zuerst gepostet (Tatsächlich)

29. Mai 2026

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

29. Mai 2026

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

21. Mai 2026

Zuletzt verifiziert

1. Mai 2026

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Schlüsselwörter

Zusätzliche relevante MeSH-Bedingungen

Andere Studien-ID-Nummern

  • USM/JEPeM/KK/24111003
  • R504-LR-GAL007-0000000410-M201 (Andere Zuschuss-/Finanzierungsnummer: MELILEA SDN BHD)

Plan für individuelle Teilnehmerdaten (IPD)

Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?

NEIN

Beschreibung des IPD-Plans

Individual participant data will not be made publicly available to protect participant confidentiality and comply with institutional and ethical regulations governing clinical research data.

Arzneimittel- und Geräteinformationen, Studienunterlagen

Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt

Nein

Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt

Nein

Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .

Klinische Studien zur Übergewichtige Erwachsene

Suchen Sie nach ähnlichen Studien

Sponsoren und Mitarbeiter

Krankheiten

Drogeninterventionen

CROs by country

CROs in China

Bedingungen

Seltene Krankheiten

Drogeninterventionen

Nahrungsergänzungsmittel

Sponsor / Mitarbeiter

Standorte

Abonnieren