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NCT07740902Completed

CHANGES IN SLEEP QUALITY AND BODY COMPOSITION FOLLOWING A MULTIMODAL LIFESTYLE INTERVENTION IN OLDER WOMEN

Source: ClinicalTrials.gov · Last updated 3 Aug 2026

Brief summary (registry, in English)

This single-arm pilot study evaluated changes in sleep quality, body composition, biochemical parameters, physical activity, and psychological well-being following a 12-week multimodal lifestyle intervention in overweight and obese women aged 60 years and older. The intervention included individualized nutrition counseling, regular psychological support, and encouragement to walk for at least 150 minutes per week. Participants were assessed at baseline and at the end of week 12. Sleep quality was evaluated using the Pittsburgh Sleep Quality Index. Secondary outcomes included anthropometric measurements, biochemical parameters, physical activity level, and psychological well-being.

Status (registry)
Completed
Study type
Interventional
Enrollment
36 (actual)
First submitted
23 Jun 2026
Start date
15 Jan 2024
Primary completion date
30 Jun 2024
Lead sponsor
Saglik Bilimleri Universitesi
Diseases
Obesity
NCT number
NCT07740902

What you commit to

  • Study type: Interventional
  • Participants enrolled: 36
  • From 15 Jan 2024 to the primary completion date, 30 Jun 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Presence of serious chronic kidney, heart, or endocrine disease

Age

  • Age under 60 years

Other

  • Inability to adhere to the nutrition program
  • Inability to adhere to the walking program
  • Following a specific diet at the time of enrollment
  • Presence of severe depressive problems

Who the study is looking for

  • Women aged 60 years or older
  • Being overweight or obese
  • Having access to nutrition counseling and psychological support services at the Healthy Living Center
  • Willingness to participate in the 12-week lifestyle intervention
  • Provision of informed consent

Age in the registry: 60 years to - · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Healthy Living Center, Karabük
Coordinator of this site? Confirm its status
KarabükTurkey (Türkiye)Unknown status

This page is information, not medical advice. Discuss any trial with your doctor.