Pulmonary Rehabilitation After Pregnancy in COVID-19 Infection: A Case Report

Sponsor
Dr. Lutfi Kirdar Kartal Training and Research Hospital (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05063799
Collaborator
(none)
1
1
1
11.2
0.1

Study Details

Study Description

Brief Summary

The 33-month pregnant patient was followed in the gynecology service with the complaint of shortness of breath after receiving the covid positive diagnosis and was transferred to the intensive care unit due to acute respiratory failure. She was intubated in the intensive care unit and the baby was taken by cesarean section. Pulmonary rehabilitation steps to be applied to the patient with long-term intensive care hospitalization will be examined.

Condition or Disease Intervention/Treatment Phase
  • Other: pulmonary rehabilitation
N/A

Detailed Description

After the patient was admitted to the chest diseases service, pulmonary rehabilitation was started. The patient was evaluated before starting pulmonary rehabilitation.

Evaluation parameters; vital signs, shortness of breath, oxygen support, grip force and pinchmeter, fatigue, anxiety and depression, cognitive functions. The pulmonary rehabilitation program will be implemented every day during the hospitalization. The pulmonary rehabilitation program will consist of breathing exercises, strengthening training of upper and lower extremity, exercises in bed, mobilization and reducing oxygen support. The patient will be re-evaluated before discharge.Pulmonary rehabilitation after discharge will continue 2-3 days a week.The patient will be re-evaluated at the 3rd, 6th, 9th and 12th months.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
1 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Pulmonary Rehabilitation After Pregnancy in COVID-19 Infection: A Case Report
Anticipated Study Start Date :
Oct 10, 2021
Anticipated Primary Completion Date :
Oct 30, 2021
Anticipated Study Completion Date :
Sep 15, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: a case included pulmonary rehabilitation program

Other: pulmonary rehabilitation
pulmonary rehabilitation programs

Outcome Measures

Primary Outcome Measures

  1. finger muscle power [15 second]

    Peripheral muscle strength will be measured with a pinchmeter

  2. grip strength [15 second]

    Peripheral muscle strength will be measured with dynamometer

Secondary Outcome Measures

  1. Assessment of cognitive [10 minutes]

    Cognitive will be assessed by Montreal Cognitive Assessment. MoCA Test; a score of 19 to 25 indicates mild cognitive impairment. Scores of between 11 and 21 suggest mild Alzheimer's disease. There is some overlap between this type of dementia and mild cognitive impairment, reflecting the difficulty in using a single test to make this type of diagnosis

  2. Assessment of anxiety and depression [10 minutes]

    Anxiety and depression will be assessed by Hospital Anxiety and Depression Scale.The HADS questionnaire has seven items each for depression and anxiety subscales. Scoring for each item ranges from zero to three, with three denoting highest anxiety or depression level. A total subscale score of >8 points out of a possible 21 denotes considerable symptoms of anxiety or depression.

  3. Assessment of fatigue [10 minutes]

    Fatigue will be assessed by Functional Assessment of Chronic Illness Therapy. The FACIT Fatigue Scale is a short, 13-item, easy to administer tool that measures an individual's level of fatigue during their usual daily activities over the past week. The level of fatigue is measured on a four point Likert scale (4 = not at all fatigued to 0 = very much fatigued)

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:

-pregnant and covid patient

Exclusion Criteria:

Contacts and Locations

Locations

Site City State Country Postal Code
1 Halime Sinem Barutcu İstanbul Turkey 34000

Sponsors and Collaborators

  • Dr. Lutfi Kirdar Kartal Training and Research Hospital

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Halime Sinem Barutçu, Physical Therapist, Dr. Lutfi Kirdar Kartal Training and Research Hospital
ClinicalTrials.gov Identifier:
NCT05063799
Other Study ID Numbers:
  • DrLutfiKirdarCH
First Posted:
Oct 1, 2021
Last Update Posted:
Oct 4, 2021
Last Verified:
Oct 1, 2021
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Halime Sinem Barutçu, Physical Therapist, Dr. Lutfi Kirdar Kartal Training and Research Hospital
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 4, 2021