Comparison of the Effects of Aerobic Exercise and Connective Tissue Massage in Postpartum Women

Sponsor
Ankara Yildirim Beyazıt University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05721625
Collaborator
(none)
40
2
12

Study Details

Study Description

Brief Summary

The aim of this study is to compare the effects of aerobic exercise and connective tissue massage on sleep, mother-infant attachment and psychological state in postpartum women.

Condition or Disease Intervention/Treatment Phase
  • Other: Aerobic exercise
  • Other: Connective tissue massage
N/A

Detailed Description

Postpartum period can affect the mental and physical health of women. Women may experience sleep problems and psychological problems due to hormonal changes and newborn care responsibilities. As a result, mother-infant attachment may also be affected. Physical activity and exercise should be encouraged in the postpartum period. It is known that aerobic exercises have positive effects on sleep and psychological problems. With the effects of connective tissue massage on the autonomic and circulatory system in the body, positive effects on sleep and psychological state can be achieved, but there are insufficient studies on this subject. In addition, no study has been found to the best of our knowledge comparing the effects of aerobic exercise and connective tissue massage in postpartum women.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
40 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Comparison of the Effects of Aerobic Exercise and Connective Tissue Massage in Postpartum Women
Anticipated Study Start Date :
Feb 15, 2023
Anticipated Primary Completion Date :
Apr 15, 2023
Anticipated Study Completion Date :
Feb 15, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: Exercise group

The aerobic exercise program will be applied at moderate intensity 3 days a week for 8 weeks. Walking will be recommended as an aerobic exercise

Other: Aerobic exercise
The aerobic exercise program will be applied at moderate intensity 3 days a week for 8 weeks. Walking will be recommended as an aerobic exercise

Active Comparator: Massage group

Connective tissue massage will be applied by the physiotherapist 3 days a week for 8 weeks. While postpartum women are in the sitting position, this massage will be applied on whole back.

Other: Connective tissue massage
Connective tissue massage will be applied by the physiotherapist 3 days a week for 8 weeks. While the patients are in the sitting position, this massage will be applied on whole back.

Outcome Measures

Primary Outcome Measures

  1. Postpartum Sleep Quality Scale [change from baseline at 8 weeks]

    In order to measure Postpartum Sleep Quality, Postpartum Sleep Quality Scale will be used. The scale includes 14 items. The lowest score that can be obtained from the scale is 0, and the highest score is 56. An increase in the score indicates a decrease in sleep quality.

Secondary Outcome Measures

  1. Mother to Infant Bonding Scale [change from baseline at 8 weeks]

    The Mother to Infant Bonding Scale, which was developed to be applied to the mother from the first day immediately after birth and allows the mother to express her feelings towards her baby in one word, will be used. This scale consists of 8 items. The lowest score that can be obtained from the scale is 0 and the highest score is 24. As the score obtained from the scale increases, the level of mother-infant attachment decreases.

  2. Edinburgh Postpartum Depression Scale [change from baseline at 8 weeks]

    The Edinburgh Postpartum Depression Scale, which was prepared for screening purposes to determine the risk of depression in postpartum women, is not intended to diagnose depression. This scale consists of 10 items. The lowest score that can be obtained from the scale is 0 and the highest score is 30. The cut-off point of the scale was calculated as 13, and women with a scale score of 13 or more were considered as the risk group.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 45 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Postpartum 6th week-1 year

  • Between the ages of 18-45

  • Being literate

Exclusion Criteria:
  • Those with orthopedic, neurological, rheumatological, mental or any systemic chronic diseases

  • Those with cardiac problems that may interfere with exercise

  • Those with suspected pregnancy

  • Those with malignancy

  • Those who have infection

  • Those who do not regularly participate in the treatment program

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Ankara Yildirim Beyazıt University

Investigators

  • Study Director: Seyda Toprak Celenay, Ankara Yildirim Beyazıt University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
seyda toprak celenay, associate professor, Ankara Yildirim Beyazıt University
ClinicalTrials.gov Identifier:
NCT05721625
Other Study ID Numbers:
  • 2023/02/01
First Posted:
Feb 10, 2023
Last Update Posted:
Feb 10, 2023
Last Verified:
Feb 1, 2023
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by seyda toprak celenay, associate professor, Ankara Yildirim Beyazıt University

Study Results

No Results Posted as of Feb 10, 2023