Geriatric Patient Care ImprovementNCT06892769
Effect of Postoperative Telehealth Counseling on Recovery and Self-Care in Geriatric Day Surgery Patients
A study testing telehealth counseling in people with Geriatric Patient Care Improvement, run by TC Erciyes University.
Trial summary
This study was planned as a randomized controlled experimental study to evaluate the effect of postoperative telehealth counseling on patient outcomes in geriatric patients undergoing day surgery. Read more about this study
- Who is it for?
- Ages 65 to 90 yearsHealthy volunteers can take part
- Conditions the study is for
- Geriatric Patient Care Improvement
- What is being tested?
- telehealth counseling
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 72 participants
- Where
- No sites listed yet
- Study dates
- 15 Mar 2025to 15 Dec 2025
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 65 to 90 years
- All sexes
- Healthy volunteers accepted
- Older adult
Who may be able to join
- 65 years of age or older,
- Having undergone day surgery (appendectomy, hernia operations, biopsy procedures, cholecystectomy...)
- No communication problems (no vision and hearing problems),
- No mental problems,
- Being able to communicate by telephone (by the patient or relative),
- Volunteering to participate in the study,
- Having at most two chronic diseases (Diabetes and Hypertension).
Who cannot join
- Surgery under emergency conditions,
- developed complications during the case
Trial locations and contacts
No sites are listed yet. Contact the study team or a site near you to ask about taking part.
Serdar Şahin contact
About this study
Official title: The Effect of Postoperative Telehealth Counseling on Postoperative Recovery and Self-care Power in Geriatric Patients Undergoing Day Surgery
This study was planned as a randomized controlled experimental study to evaluate the effect of postoperative telehealth counseling on patient outcomes in geriatric patients undergoing day surgery.
Hypotheses of the Study H11: In geriatric patients undergoing day surgery, the postoperative self-care power of the intervention group receiving postoperative telehealth counseling is higher than the control group not receiving counseling.
Read more
H12: In geriatric patients undergoing day surgery, the postoperative recovery status of the intervention group receiving postoperative telehealth counseling is higher than that of the control group not receiving counseling.
Inclusion Criteria;
- 65 years of age or older,
- Having undergone day surgery (appendectomy, hernia operations, biopsy procedures, cholecystectomy...)
- No communication problems (no vision and hearing problems),
- No mental problems,
- Being able to communicate by telephone (by the patient or relative),
- Volunteering to participate in the study,
- Having at most two chronic diseases (Diabetes and Hypertension).
Exclusion Criteria;
- Surgery in emergency conditions,
- developed complications during the case
Read the detailed description
Data Collection Forms Patient Information Form: The form, prepared by the researchers with the support of the literature, includes a total of twelve questions questioning sociodemographic characteristics (age, gender, educational status, marital status, smoking, alcohol use, comorbidity, height, weight, body mass index and surgical experience) and disease-related characteristics (surgical procedure performed) Postoperative Recovery Index (PRAI): TThe index consists of 5 sub-dimensions and 25 items. The sub-dimensions are psychological symptoms, physical activities, general symptoms, bowel symptoms and craving symptoms. When determining the sub-dimension score, the scores of the related items are summed and their arithmetic averages are taken. For the total score, all items are summed and the arithmetic mean is taken. Higher scores on the index reflect more difficulty in postoperative recovery, while lower scores indicate that postoperative recovery is easier. In Cengiz and Aygin's study, the Cronbach's alpha value of the ASIQ was determined as 0.96 (Cengiz, 2018).
Self-Care Power Scale: It was developed by Kearney and Fleischer in 1979. The scale, which is used to determine the ability and power of people to take care of themselves, consists of 35 statements (items). The maximum score is 140. The higher the score obtained from the scale, the higher the self-care or self-care ability and power of the individual. The cronbach alpha value of the scale is 0.92 Data Collection The investigator evaluated the patients admitted to the clinic with the decision of surgery according to the research criteria. The surgery date and intensive care processes of the patients planned to be included were followed. Patients who were visited in the clinic before discharge were verbally informed about the study in face-to-face interviews of 10-15 minutes with the patient's relatives in the room, and informed consent forms were signed. It was reported that the data would be collected by the researcher through face-to-face interviews.
- Patient identification form will be filled out
- Contact information (telephone) of the patients will be taken and contact information (telephone) of the researcher will be given to the patients/relatives
- Patients/relatives will be informed that they can receive telephone counseling services from the researcher for the problems they experience in home care processes
- In line with the "Discharge Training Guide" prepared by the researcher in line with the literature, discharge training will be given to the patients and their relatives once in the patient's room by meeting face-to-face for an average of 15-20 minutes.
- In the 1st and 4th week after discharge, patients will be called by the researcher by phone and counseling services will be provided again.
- Postoperative Recovery Index and Self-Care Power Scale will be completed every week. The study will be terminated in the 4th week.
Control Group Practices
- Patients who meet the sample selection criteria will be informed about the study and their verbal and written consent will be obtained by reading the voluntary information form
- Patient identification form will be filled out
- Contact information (telephone) of the patients will be obtained.
- In line with the "Discharge Training Guide" prepared by the researcher in line with the literature, discharge training will be given to the patients and their relatives once in the patient's room by meeting face to face for an average of 15-20 minutes.
- At the 1st and 4th week after discharge, the patients will be called by the researcher by phone and the Postoperative Recovery Index and Self-Care Power Scale will be filled out. The study will be finalized in the 4th week.
- Conditions
- Geriatric Patient Care Improvement
- Being tested
- telehealth counseling
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
telehealth counselingOther
Patients in the intervention group will be called every week (for 4 weeks) and will be trained in line with the determined guide and scales will be filled.
| Study group | Role | What they receive |
|---|---|---|
| Routine care | No intervention | Patients will only be called weekly to complete the scales. |
| telehealth counseling application | Experimental | to provide active counseling by calling weekly by phone on issues that the patient needs Receives: Other: telehealth counseling |
What is being measured
The primary outcome is the main question the study is designed to answer.
Postoperatıve recovery process
Data collection tools
Postoperative Recovery Index (PRAI): The index consists of 5 sub-dimensions and 25 items. The sub-dimensions are psychological symptoms, physical activities, general symptoms, bowel symptoms and craving symptoms. When determining the sub-dimension score, the scores of the related items are summed and their arithmetic averages are taken. For the total score, all items are summed and the arith.
Maximum Possible Score:
If the scoring system for each item is on a scale (for example, 1 to 5), the maximum score for each sub-dimension would be the sum of the highest possible score for each item within that sub-dimension. The total maximum score is the sum of the maximum scores for all 25 items.
If each item can score between 1 and 5, the maximum score per item is 5. Maximum score for 25 items: 5 x 25 = 125 (total score)
Minimum Possible Score:
The minimum score for each item is 1, so the lowest possible score for each sub-dimension is 25 (1 for each of the 25 ite
Measured: postoperative 1st, 2nd, 3rd, 4th week
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted25 Mar 2025
- Study start15 Mar 2025 (estimated)
- Primary completion15 Nov 2025 (estimated)
- Study completion15 Dec 2025 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Geriatric Patient Care ImprovementStudies of the same condition, open and under way.
- More trials run by TC Erciyes UniversityThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Supportive care
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind
- Who is masked
- Outcomes assessor
- Enrolment
- 72 participants (estimated)
Sponsor and investigators
- Lead sponsor
- TC Erciyes University
- Sponsor type
- University, hospital or other
- Collaborators
- Kirsehir Ahi Evran Universitesi
- Responsible party
- Principal investigator, Dilek Talhaoglu, TC Erciyes University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06892769
- Sponsor's protocol ID
- Geriatric surgery
- Status last verified
- Mar 2025
- First submitted
- 9 Mar 2025
- Last updated
- 25 Mar 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 25 Mar 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- The Effect of Postoperative Telehealth Counseling on Postoperative Recovery and Self-care Power in Geriatric Patients Undergoing Day Surgery
- ClinicalTrials.gov ID
- NCT06892769
- Acronym / sponsor ID
- Geriatric surgery
- Conditions
- Geriatric Patient Care Improvement
- Study type
- Interventional
- Recruitment status
- Not yet recruiting
- Enrolment
- 72 participants (estimated)
- Lead sponsor
- TC Erciyes UniversityUniversity, hospital or other
- Collaborators
- Kirsehir Ahi Evran Universitesi
- Study start
- 15 Mar 2025 (estimated)
- Primary completion
- 15 Nov 2025 (estimated)
- Study completion
- 15 Dec 2025 (estimated)
- First posted
- 25 Mar 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This study was planned as a randomized controlled experimental study to evaluate the effect of postoperative telehealth counseling on patient outcomes in geriatric patients undergoing day surgery.
Hypotheses of the Study H11: In geriatric patients undergoing day surgery, the postoperative self-care power of the intervention group receiving postoperative telehealth counseling is higher than the control group not receiving counseling.
H12: In geriatric patients undergoing day surgery, the postoperative recovery status of the intervention group receiving postoperative telehealth counseling is higher than that of the control group not receiving counseling.
Inclusion Criteria;
- 65 years of age or older,
- Having undergone day surgery (appendectomy, hernia operations, biopsy procedures, cholecystectomy...)
- No communication problems (no vision and hearing problems),
- No mental problems,
- Being able to communicate by telephone (by the patient or relative),
- Volunteering to participate in the study,
- Having at most two chronic diseases (Diabetes and Hypertension).
Exclusion Criteria;
- Surgery in emergency conditions,
- developed complications during the case
Detailed description
Data Collection Forms Patient Information Form: The form, prepared by the researchers with the support of the literature, includes a total of twelve questions questioning sociodemographic characteristics (age, gender, educational status, marital status, smoking, alcohol use, comorbidity, height, weight, body mass index and surgical experience) and disease-related characteristics (surgical procedure performed) Postoperative Recovery Index (PRAI): TThe index consists of 5 sub-dimensions and 25 items. The sub-dimensions are psychological symptoms, physical activities, general symptoms, bowel symptoms and craving symptoms. When determining the sub-dimension score, the scores of the related items are summed and their arithmetic averages are taken. For the total score, all items are summed and the arithmetic mean is taken. Higher scores on the index reflect more difficulty in postoperative recovery, while lower scores indicate that postoperative recovery is easier. In Cengiz and Aygin's study, the Cronbach's alpha value of the ASIQ was determined as 0.96 (Cengiz, 2018).
Self-Care Power Scale: It was developed by Kearney and Fleischer in 1979. The scale, which is used to determine the ability and power of people to take care of themselves, consists of 35 statements (items). The maximum score is 140. The higher the score obtained from the scale, the higher the self-care or self-care ability and power of the individual. The cronbach alpha value of the scale is 0.92 Data Collection The investigator evaluated the patients admitted to the clinic with the decision of surgery according to the research criteria. The surgery date and intensive care processes of the patients planned to be included were followed. Patients who were visited in the clinic before discharge were verbally informed about the study in face-to-face interviews of 10-15 minutes with the patient's relatives in the room, and informed consent forms were signed. It was reported that the data would be collected by the researcher through face-to-face interviews.
- Patient identification form will be filled out
- Contact information (telephone) of the patients will be taken and contact information (telephone) of the researcher will be given to the patients/relatives
- Patients/relatives will be informed that they can receive telephone counseling services from the researcher for the problems they experience in home care processes
- In line with the "Discharge Training Guide" prepared by the researcher in line with the literature, discharge training will be given to the patients and their relatives once in the patient's room by meeting face-to-face for an average of 15-20 minutes.
- In the 1st and 4th week after discharge, patients will be called by the researcher by phone and counseling services will be provided again.
- Postoperative Recovery Index and Self-Care Power Scale will be completed every week. The study will be terminated in the 4th week.
Control Group Practices
- Patients who meet the sample selection criteria will be informed about the study and their verbal and written consent will be obtained by reading the voluntary information form
- Patient identification form will be filled out
- Contact information (telephone) of the patients will be obtained.
- In line with the "Discharge Training Guide" prepared by the researcher in line with the literature, discharge training will be given to the patients and their relatives once in the patient's room by meeting face to face for an average of 15-20 minutes.
- At the 1st and 4th week after discharge, the patients will be called by the researcher by phone and the Postoperative Recovery Index and Self-Care Power Scale will be filled out. The study will be finalized in the 4th week.
Study design
- Primary purpose
- Supportive care
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (outcomes assessor)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Routine care | No intervention | –Patients will only be called weekly to complete the scales. |
| telehealth counseling application | Experimental | Other: telehealth counselingto provide active counseling by calling weekly by phone on issues that the patient needs |
Who may qualify
- Ages
- 65 to 90 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Older adult
Key inclusion criteria (7 listed)
- 65 years of age or older,
- Having undergone day surgery (appendectomy, hernia operations, biopsy procedures, cholecystectomy...)
- No communication problems (no vision and hearing problems),
- No mental problems,
- Being able to communicate by telephone (by the patient or relative),
Key exclusion criteria (2 listed)
- Surgery under emergency conditions,
- developed complications during the case
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| telehealth counselingPatients in the intervention group will be called every week (for 4 weeks) and will be trained in line with the determined guide and scales will be filled. | Other | telehealth counseling application |
Primary outcome
Postoperatıve recovery process
Time frame: postoperative 1st, 2nd, 3rd, 4th week
Data collection tools Postoperative Recovery Index (PRAI): The index consists of 5 sub-dimensions and 25 items. The sub-dimensions are psychological symptoms, physical activities, general symptoms, bowel symptoms and craving symptoms. When determining the sub-dimension score, the scores of the related items are summed and their arithmetic averages are taken. For the total score, all items are summed and the arith. Maximum Possible Score: If the scoring system for each item is on a scale (for example, 1 to 5), the maximum score for each sub-dimension would be the sum of the highest possible score for each item within that sub-dimension. The total maximum score is the sum of the maximum scores for all 25 items. If each item can score between 1 and 5, the maximum score per item is 5. Maximum score for 25 items: 5 x 25 = 125 (total score) Minimum Possible Score: The minimum score for each item is 1, so the lowest possible score for each sub-dimension is 25 (1 for each of the 25 ite
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 25 Mar 2025.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Serdar Şahin contact
Questions about this trial
What is this clinical trial studying?
A study testing telehealth counseling in people with Geriatric Patient Care Improvement, run by TC Erciyes University.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 7 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: opening soon, as of the sponsor's last update on 25 Mar 2025. Status can change between updates, so confirm with the study contact before making plans.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Dilek TALHAOĞLU (+905545911691, dilektalhaoglu@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Postoperatıve recovery process (time frame: postoperative 1st, 2nd, 3rd, 4th week). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 25 Mar 2025.