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the effect of cycle of exercises on pregnancy outcomes

Investigation of the effect of a cycle of exercises on pregnancy outcomes in Primigravida Women

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201403167497N3
Enrollment
120
Registered
2016-02-18
Start date
2015-04-21
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Condition 1: delivery. Condition 2: delivery. Condition 3: delivery. Condition 4: delivery. Single spontaneous delivery Single delivery by caesarean section Single delivery by forceps and vacuum extractor Other assisted single delivery

Interventions

Intervention 1: The intervention group subjects were required to do aerobic exercises 30 minutes a day, three days a week for 8 weeks. Aerobic exercise program started with 5 minutes warming, continue
such a way that their heartbeat would not exceed 140 beats per minute (bpm) the control group mothers only received the routine pregnancy care. Intervention 2: The control group participants, on the
Behavior
The intervention group subjects were required to do aerobic exercises 30 minutes a day, three days a week for 8 weeks. Aerobic exercise program started with 5 minutes warming, continued with the main
such a way that their heartbeat would not exceed 140 beats per minute (bpm) the control group mothers only received the routine pregnancy care
The control group participants, on the other hand, only received the routine care without performing aerobic exercises.

Sponsors

Vice Chancellor for research of Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: primiparous ;18-35 years old; gestational age of 20 weeks ; singleton pregnancy ; being primiparous; not having the history of pregnancy complications; not having the history of doing professional sports; and normal Body Mass Index (BMI=20-25 ) Exclusion criteria: were suffering from underlying diseases; such as hypertension ; thyroid disorders; women’s or pregnancy disorders; diabetes; epilepsy;cardiovascular diseases; renal disorders; and pulmonary diseases; having known pregnancy complications; such as polyhydramnios; oligohydramnios; placenta previa;detachment; known fetal disorders; intrauterine death; cervical insufficiency;history of infertility; bleeding during pregnancy; and pain; having limitations for doing physical activities; and not being willing to participate in the study. .

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Duration of pregnancy. Timepoint: After delivery. Method of measurement: Chart.;Type of delivery. Timepoint: after intervention. Method of measurement: chart.;Apgar scor. Timepoint: after intervention. Method of measurement: Chart.;Back pain. Timepoint: after intervention. Method of measurement: visual scale of pain.

Secondary

MeasureTime frame
Assess back pain. Timepoint: The begain of intervention and after intervention. Method of measurement: the 10 point Visual Analog Scale (VAS).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMonireh toosi

Zand street, Shiraz University of Medical Sciences ,shiraz

Toosim_m@yahoo.com+98 71 1647 4258

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026