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RecruitingNCT07659925T2DM_NLPUpdated Jun 22, 2026

Periodization-Based Strength Exercise Training in İndividuals With Type 2 Diabetes

An interventional study of Non-linear Periodization-Based Strength Training and Linear Periodization-Based Strength Training in Type 2 Diabetes, sponsored by Baskent University. Recruiting at 1 site in Turkey (Türkiye). Open to participants aged 18 Years to 65 Years. Per ClinicalTrials.gov, last updated 2026-06-22.

Sponsored by Baskent University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Started May 2026; still recruiting 6 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
48
Allocation
Randomized
Ages
18 Years to 65 Years
Sex
All
01

Study summary

This randomized controlled study aims to compare the effects of different periodization-based strength training approaches in individuals with type 2 diabetes mellitus. Participants will be allocated to non-linear periodization, linear periodization, or control groups. The intervention program will be conducted for 8 weeks and will evaluate exercise capacity, muscle strength, quality of life, body composition, and metabolic parameters.

Read the detailed description

Type 2 diabetes mellitus is associated with reduced exercise capacity, decreased muscle strength, impaired quality of life, and metabolic dysfunction. Exercise training is recommended as an important component of diabetes management; however, the comparative effectiveness of different strength training periodization approaches remains unclear.

This randomized controlled trial aims to compare the effects of non-linear periodization and linear periodization strength training programs in individuals with type 2 diabetes mellitus. Participants will be randomized into three groups: a non-linear periodization training group, a linear periodization training group, and a control group receiving usual care.

The intervention will be conducted for 8 weeks, three times per week. Outcomes including exercise capacity, muscle strength, body composition, quality of life, and metabolic parameters will be evaluated before and after the intervention period.

02

Conditions studied

  • Type 2 Diabetes

Keywords

  • Type 2 Diabetes Mellitus
  • Strength Training
  • Non-linear Periodization
  • Exercise Capacity
  • Muscle Strength
  • Quality of Life
  • Linear Periodization
  • Resistance Training
03

In context

Diabetes Mellitus, Type 2

10,371 studies on the registry are indexed under Diabetes Mellitus, Type 2; 1,406 are open to participants now.

This study's planned enrollment of 48 is below the median of 80 across 8,350 interventional studies indexed under Diabetes Mellitus, Type 2.

Browse Diabetes Mellitus, Type 2 studies →

Lead sponsor

Baskent University is the lead sponsor of 209 studies on the registry; 35 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Adults aged between 18 to 65 years
  • Diagnosis of Type 2 Diabetes Mellitus (T2DM)
  • Not having participated in any structured exercise program within the last 6 months
  • Willingness to participate in the study and provide written

Exclusion criteria

Exclusion Criteria:

  • Presence of nephropathy, retinopathy, or peripheral neuropathy
  • Presence of neurological, cognitive, or orthopedic disorders that may affect outcome measurements
  • Severe respiratory disease ( [FEV1] \<35% or Forced Vital Capacity [FVC] \<50%)
  • Presence of ischemic heart disease or peripheral arterial disease
  • History of any cardiovascular event within the last 6 months
  • Current
Terms in these criteria, in plain language(3)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

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You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

FEV1

From a breathing test (spirometry): how much air you can blow out in the first second. Often given as a percentage of what is expected for your age, height and sex.

Cancer (malignancy)

Malignancy means cancer. Criteria about another or earlier malignancy ask whether you have had a different cancer, usually within a set number of years.

Some are commonly allowed, such as treated skin cancers other than melanoma and early cancers removed completely — check the exceptions this study lists.

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
48 participants (estimated)

Study arms

  • Experimental
    Non-linear Periodization Group

    Participants will receive non-linear periodization-based strength training three times per week for 8 weeks.

    Behavioral: Non-linear Periodization-Based Strength Training

  • Experimental
    Linear Periodization Group

    Participants will receive linear periodization-based strength training three times per week for 8 weeks.

    Behavioral: Linear Periodization-Based Strength Training

  • Active comparator
    Control Group

    Participants will receive usual care and no structured exercise intervention during the study period.

    Other: Usual Care

Interventions

  • BehavioralNon-linear Periodization-Based Strength Training

    Participants will perform supervised non-linear periodization-based strength training three times per week for 8 weeks.

  • BehavioralLinear Periodization-Based Strength Training

    Participants will perform supervised linear periodization-based strength training three times per week for 8 weeks.

  • OtherUsual Care

    Participants will receive usual care and no structured exercise intervention during the study period.

06

What researchers measure

Primary outcomes

  1. Exercise Capacity

    Exercise capacity will be assessed using the 6-Minute Walk Test (6MWT)

    Time frame: Baseline and after 8 week

Secondary outcomes

  1. Change in Peripheral Muscle Strength

    Peripheral muscle strength will be assessed using handheld dynamometry for upper and lower extremity muscle groups and reported in Newton (N).

    Time frame: Baseline and after 8 weeks

  2. Change in Hand Grip Strength

    Hand grip strength will be assessed using a hand dynamometer and reported in kilograms (kg).

    Time frame: Baseline and after 8 weeks

  3. Change in Diabetes Quality of Life Questionnaire Score

    Change in the Turkish version of the Diabetes Quality of Life Questionnaire (DQOL) total score and subscale scores from baseline to 8 weeks will be evaluated. The DQOL consists of 45 items assessing treatment satisfaction, psychological impact, concerns about future effects of diabetes, and social/vocational concerns. Each item is scored on a 1-5 scale, and higher scores indicate better diabetes-related quality of life.

    Time frame: Baseline and after 8 weeks

  4. Change in Body Fat Percentage

    Body fat percentage (%) will be assessed using bioelectrical impedance analysis (BIA).

    Time frame: Baseline and after 8 weeks

  5. Change in Skeletal Muscle Mass

    Skeletal muscle mass (kg) will be assessed using bioelectrical impedance analysis (BIA).

    Time frame: Baseline and after 8 weeks

  6. Change in Resting Metabolic Rate

    Resting metabolic rate (kcal/day) will be assessed using indirect calorimetry (COSMED Fitmate Pro, Rome, Italy).

    Time frame: Baseline and after 8 weeks

  7. Change in Hemoglobin A1c (HbA1c)

    Glycemic control will be assessed by measuring glycated hemoglobin (HbA1c) levels (%).

    Time frame: Baseline and after 8 weeks

  8. Change in Fasting Blood Glucose

    Glycemic control will be assessed by measuring fasting blood glucose levels (mg/dL).

    Time frame: Baseline and after 8 weeks

07

Study locations

1 of 1 sites recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 22, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07659925
Lead sponsor
Baskent University
Responsible party
Neslihan Duruturk (Prof. Dr., Baskent University) — Principal investigator
First posted
Jun 22, 2026
Start date
May 1, 2026
Primary completion
Nov 2026 (estimated)
Completion
Dec 2026 (estimated)
Last update
Jun 22, 2026

Study contacts

Ayşegül Erkoç, PT
Contact
erkcaysegl@gmail.com
+90 553-301-36-73
Neslihan Duruturk, PhD
principal investigator · Baskent University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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