NCT07717333

Brief Summary

This prospective observational study aims to evaluate longitudinal changes in sarcopenia-related parameters in patients undergoing bariatric surgery. Obesity and rapid weight loss following bariatric surgery may lead to changes in muscle mass, muscle strength, and physical performance, which are important components of sarcopenia. Participants will be evaluated before bariatric surgery and during postoperative follow-up visits. Muscle thickness will be assessed using ultrasonography of the femoral muscles. Muscle strength and physical performance will be evaluated using handgrip strength, the 5-meter walk test, and the five-times sit-to-stand test. The study aims to investigate the effects of bariatric surgery on muscle function and physical performance over time and to contribute to the early identification of sarcopenia risk in this patient population.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
80

participants targeted

Target at P50-P75 for all trials

Timeline
11mo left

Started Apr 2026

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress25%
Apr 2026Jun 2027

Study Start

First participant enrolled

April 10, 2026

Completed
1 month until next milestone

First Submitted

Initial submission to the registry

May 24, 2026

Completed
2 months until next milestone

First Posted

Study publicly available on registry

July 21, 2026

Completed
10 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 30, 2027

Expected
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

June 30, 2027

Last Updated

July 21, 2026

Status Verified

July 1, 2026

Enrollment Period

1.1 years

First QC Date

May 24, 2026

Last Update Submit

July 16, 2026

Conditions

Outcome Measures

Primary Outcomes (1)

  • Change in Femoral Muscle Thickness

    Femoral muscle thickness will be assessed using ultrasonography before bariatric surgery and during postoperative follow-up visits to evaluate longitudinal changes associated with sarcopenia.

    Preoperative baseline, postoperative 1st month, 3rd month, 6th month, and 12th month assessments

Secondary Outcomes (2)

  • Change in Handgrip Strength

    Preoperative baseline, postoperative 1st month, 3rd month, 6th month, and 12th month assessments

  • Change in Five-Times Sit-to-Stand Test Performance

    Preoperative baseline, postoperative 1st month, 3rd month, 6th month, and 12th month assessments

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Adult patients scheduled to undergo bariatric surgery at the study center will be included in this prospective observational study. Participants will be evaluated before surgery and during postoperative follow-up visits to assess longitudinal changes in muscle thickness, muscle strength, and physical performance related to sarcopenia.

You may qualify if:

  • Adults aged 18 years and older
  • Patients scheduled to undergo bariatric surgery
  • Ability to participate in physical performance tests
  • Ability to provide written informed consent

You may not qualify if:

  • Presence of neurological or musculoskeletal disorders affecting muscle strength or physical performance
  • Severe cardiopulmonary disease limiting physical activity
  • Active malignancy
  • Pregnancy
  • Inability to complete study assessments
  • Refusal to participate in the study

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Kanuni Sultan Suleyman Education and Research Hospital

Istanbul, KÜÇÜKÇEKMECE, 34307, Turkey (Türkiye)

RECRUITING

MeSH Terms

Conditions

ObesitySarcopenia

Condition Hierarchy (Ancestors)

OverweightOvernutritionNutrition DisordersNutritional and Metabolic DiseasesBody WeightSigns and SymptomsPathological Conditions, Signs and SymptomsMuscular AtrophyNeuromuscular ManifestationsNeurologic ManifestationsNervous System DiseasesAtrophyPathological Conditions, Anatomical

Central Study Contacts

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

May 24, 2026

First Posted

July 21, 2026

Study Start

April 10, 2026

Primary Completion (Estimated)

May 30, 2027

Study Completion (Estimated)

June 30, 2027

Last Updated

July 21, 2026

Record last verified: 2026-07

Data Sharing

IPD Sharing
Will not share

Individual participant data will not be publicly shared in order to protect participant confidentiality and privacy. De-identified data may be available from the investigators upon reasonable request.

Locations