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

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age20-45
SponsorMiddle East University

About this trial

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

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Diagnosis of type 1 diabetes for more than 5 years

Unchanged insulin doses for no less than three months

Good glycemic control, defined as glycated hemoglobin levels below 7%

Minimal to moderate depressive symptoms

Disqualifiers

None

Trial design

Design model

Parallel

Treatments tested in this trial

  • Resistance exercises

    Other intervention

    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.

  • Breathing exercises

    Other intervention

    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.

Treatment groups

78 Participants
are divided into 2 treatment groups
Group A: Resistance training groupActive comparator 2 interventions
Group B: Control groupActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Depression

Depression will be assessed using the Beck Depression Inventory-II

Time frame
Baseline and 12 weeks later

Secondary outcomes

1

Sleep quality

Sleep quality will be assessed using the Pittsburgh Sleep Quality Index

Time frame
At baseline and 12 weeks later
2

Quality of life

The Arabic version of the Diabetes Quality of Life Questionnaire will be completed by each participant to assess quality of life

Time frame
At baseline and after 12 weeks

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

This trial is not recruiting at the moment. You can still explore other options: