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Resistance Training on Depression and Quality of Life in Type 1 Diabetic Women

Effect of Resistance Training on Depression and Quality of Life in Type 1 Diabetic Women

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07466186
Enrollment
78
Registered
2026-03-12
Start date
2026-03-18
Completion date
2026-07-28
Last updated
2026-03-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Type 1 Diabetes Mellitus

Brief summary

Find out the effects of resistance training on depression, sleep quality, and quality of life in women with type 1 diabetes mellitus

Detailed description

Seventy-eight women aged 20 to 45 years with type 1 diabetes mellitus will be randomly assigned to either a resistance training group, which will receive both resistance and breathing exercises, or an active control group, which will receive breathing exercises only. The intervention will last for 12 weeks, with resistance exercises will be performed at moderate intensity. Outcomes will be assessed using the Beck Depression Inventory-II, the Pittsburgh Sleep Quality Index, and the Diabetes Quality of Life Questionnaire.

Interventions

The program will include seven exercises targeting major muscle groups: chest press, triceps extension, and shoulder front raise for the upper limbs; back extensions and abdominal crunches for the trunk; and leg press, leg curl, and calf raise for the lower limbs.

OTHERBreathing exercises

The procedure will be first demonstrated and explained to each woman prior to the first session. Starting from a crook-lying position, participants will be guided to inhale through the nose for a count of four, hold their breath for another four counts, exhale slowly through the mouth over four counts, and then pause for an additional four counts before repeating the cycle.

Sponsors

Middle East University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
20 Years to 45 Years
Healthy volunteers
No

Inclusion criteria

1. Diagnosis of type 1 diabetes for more than 5 years 2. Unchanged insulin doses for no less than three months 3. Good glycemic control, defined as glycated hemoglobin levels below 7% 4. Minimal to moderate depressive symptoms 5. Sleep quality impairment

Exclusion criteria

Presence of other types of diabetes, unstable cardiopulmonary conditions, recent neurological or musculoskeletal problems affecting exercise, pregnancy, postmenopausal status, and the use of sedatives or antidepressants.

Design outcomes

Primary

MeasureTime frameDescription
DepressionBaseline and 12 weeks laterDepression will be assessed using the Beck Depression Inventory-II

Secondary

MeasureTime frameDescription
Sleep qualityAt baseline and 12 weeks laterSleep quality will be assessed using the Pittsburgh Sleep Quality Index
Quality of lifeAt baseline and after 12 weeksThe Arabic version of the Diabetes Quality of Life Questionnaire will be completed by each participant to assess quality of life

Countries

Egypt

Contacts

CONTACTSaher Elgayar, Ph.D
saherlotfy020@gmail.com+201020429911
CONTACTMohammed Elhamrawy, Ph.D
STUDY_DIRECTORMohamed Saif

National institute for Gerontology

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 13, 2026