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Frontiers in Endocrinology logoLink to Frontiers in Endocrinology
. 2019 Jun 12;10:380. doi: 10.3389/fendo.2019.00380

The Effect of Cognitive-Behavioral Therapy on Acromegalics After a 9-Month Follow-Up

Lia Silvia Kunzler 1,*, Luciana Ansaneli Naves 2, Luiz Augusto Casulari 3,4
PMCID: PMC6581695  PMID: 31244782

Abstract

Introduction: The quality of life of acromegalics is compromised. Treatment with the “Think healthy and feel the difference” technique has been described as effective in the improvement of the quality of life of these patients in the short term. However, its effectiveness in the long term needs to be evaluated.

Objective: The purpose of this study was to evaluate whether the good results obtained from the “Think healthy and feel the difference” technique in the short term persists in the long term, after the end of the treatment.

Method: This is a non-randomized longitudinal study with 23 acromegalic divided into two groups: an intervention group with 10 patients and a control group with 13 patients. The intervention itself covered nine group sessions, organized weekly, using a technique called “Think healthy and feel the difference.” The control group did not receive the aforementioned treatment. The Short Form 36 Question Health Survey (SF-36) and the Beck Depression Inventory were administered before the sessions began, at the end of the nine therapy sessions and at the 9-month follow-up.

Results: At the end of the treatment, the results of the SF-36 showed improvement in the mental health of the intervention group compared to the control group. The effects of therapy were maintained at the 9 month follow-up.

Conclusion: Cognitive-behavioral therapy, applied in a group format, can improve the quality of life of acromegalic patients in the short- and long-term.

Keywords: acromegaly, cognitive-behavioral therapy, quality of life, follow-up, SF−36

Introduction

In acromegaly, prolonged exposure to growth hormone (GH) and insulin-like growth factor (IGF-1) is associated with worsening comorbidities and impairment in quality of life (1). Biochemical dysregulation of the disease can reduce acromegalic life expectancy by up to 10 years (1, 2), but, when the disease is controlled, mortality may reach parity with the normal population (2). Despite this, biochemical control of acromegaly through currently available treatments—transsphenoidal surgery, radiotherapy and pharmacotherapy—has been insufficient to improve quality of life (24).

In addition to clinical complications, orofacial changes and orthopedic comorbidities can also impair the quality of both functional and social life (1). Acromegalics show a preoccupation with the performance of tasks involved in executive dysfunction syndrome, which may impair the execution of everyday tasks (5), as well as jeopardize the development of effective coping strategies (6). Receptors for GH and IGF-1 are present in the central nervous system, especially in the limbic system and frontal lobe. An excess of GH and IGF-1 results in cognitive impairment may be irreversible, as in valvulopathy and arthropathy (6).

Delay in diagnosis is related to social isolation, distortion of body image, and depression, with consequent psychosocial impairment (1, 7). The impairment in quality of life may also be related to psychiatric comorbidities, such as anxiety, cognitive impairment, and depression, more frequently than in other somatic diseases (1, 8).

Therefore, quality of life impairment may be related to psychopathology and not only to biochemical dysregulation of the disease (3). Cognitive dysfunctions due to emotional imbalance have been observed in acromegalics, especially in executive functions and in memory (5, 9, 10). Lower activation of areas of the brain strongly associated with cognitive functions—the prefrontal and temporal cortex—has been observed as well (5).

Considering the importance of psychopathology in acromegaly (3), particularly, related to the supposed irreversible effect of excess GH on mood and behavior (1), acromegalics can benefit from psychotherapeutic treatment (2, 8, 9). However, no results on the effects of psychotherapy on improvement of quality of life in acromegalics had been published until recently, despite being well-established for other chronic diseases (4).

In this context, cognitive-behavioral therapy (CBT) can be applied to cases of acromegaly. Over the years, research involving CBT has contributed to clinical practice, since improvements in techniques favor its application in different clinical contexts (11). More than 300 research studies have applied CBT to various diseases, as it is an effective intervention with a low cost (12).

Initially, the cognitive model, proposed by Aaron Beck in the 1960s, was based on the cognitive distortions present in depression (13). Depressive content was characterized by low self-esteem and guilt with a consequent desire for isolation (14). In CBT, thought, emotion, and behavior are intertwined (14, 15).

The cognitive model has been adapted for various diseases. In this model, schemas are sets of beliefs associated with greater emotional imbalance (13, 16, 17). Due to facial changes and growth of their hands and feet, (1), acromegalics can present schemas of inadequacy, devaluation and failure. As with acromegalics, depressed patients overestimate their defects, failures, and problems, and tend to underestimate or ignore any favorable traits, skills, or achievements (14).

The cognitive conceptualization of each case is facilitated by Socratic questioning. The therapist formulates questions to help the patient understand the effects of emotions and thoughts on behavior. Such questioning aims at developing new coping perspectives from the learning process (18).

Among several clinical applications, in social phobia, for example, the patient feels threatened in social situations, thinking “If I try to talk, I'll look stupid”; as a result the patient avoids social interaction (13). In acromegaly, because of their physical appearance, the cognitive model may be similar, based on the belief: “If I look horrible, everyone will stare and criticize me.”

Uncertainty, cost and benefit assessment, and perceived risk precede the choice of a given behavior, and require some degree of flexibility (19). Despite the importance of decision making, not much research has been carried out the influence of emotional imbalance on choices (20). In the brain, activation of the cingulate cortex and the amygdala is important because of their role in emotional regulation, which is one of the main objectives of CBT (21, 22).

In this context, the “Think healthy” technique was applied in a group setting with the aim of improving the quality of life of acromegalics (23). The technique is composed of six stages and uses the figures of gray and green avocados to represent problems and possible coping alternatives (23). One of its fundamental principles is decision making toward healthy behaviors, facilitated by the following thought: “Despite the negative repercussions of acromegaly, what can I do that is healthier toward thinking and behavior?”

In a previously published study, we showed that CBT, with the “Think Healthy” technique, significantly improved the quality of life of acromegalics; evaluated by the SF-36 in the areas of general health (d′ = −0.264, p = 0.031) and mental health (d′ = −1.123, p = 0.012). In the dimensions of physical and emotional aspects there were no significant improvement, although four of the five patients with floor effects did improve (23).

The aim of the present study is to evaluate whether the initially obtained results were still present after 9 months from the end of the treatment. It also compares whether, after that period of time, the treatment group shows any difference to the control group that did not receive the treatment at the same time.

Methods

This was a non-randomized longitudinal study performed on acromegalics attending the neuroendocrinology outpatient clinic of the University Hospital of Brasília in the period from September 2015 to November 2016.

The following inclusion criteria were used: patients with acromegaly in follow-up at the above-mentioned clinic, males and females, aged between 18 and 75 years; intellectual capacity to follow the intervention; and agreement to participate in the study. The exclusion criterion was risk of suicide, evaluated according to the response to item 9 of the BDI (24).

The meetings were held in a space that comfortably accommodated the number of participants, arranged in a circle, with the possibility of handling the material, taking notes and completing exercises. The room was well lit, cool, and had good privacy.

The clinical trial was registered in a public trial registry, and the accession number is UTN—U 1111-1220-9846. The research project was approved by the Research Ethics Committee (CEP) of the Faculty of Health Sciences of the University of Brasília—UnB. A Free and Informed Consent form was read and signed by the participants of the group.

Sample Composition and Evaluation Steps

One week before the start of group therapy, which was considered the pre-intervention stage, the work proposal, the dates scheduled for the meetings, and the content scheduled for each session were provided. Information was collected about age, gender, time, and activity of the disease, arterial hypertension, diabetes, arthralgia, and type of acromegaly treatment—surgery, radiotherapy and/or oral or injectable medication.

The disease was considered active when IGF-1 was above the normal value for age and gender, even when using cabergoline, octreotide, or pegvisomant; considered controlled when the use of these drugs kept blood concentrations of IGF-1 within the normal range; and considered cured when the concentrations of this hormone were within the normal range without the use of these drugs. Hypertensive participants were considered as those with blood pressure equal to or >140 × 90 mmHg, or those using anti-hypertensive drugs (25). A participant was considered to have diabetes mellitus type 2 when glycemia was equal to or higher than 125 mg/dL, or 2 h post oral glucose tolerance test higher than 199 mg/dL or HbA1 levels equal to or higher 6.5%, or if he/she was using hypoglycemic drugs (26).

The groups were selected according to convenience, availability, and the choice of each participant. Patients of the control group did not participate on this phase of the research due to the distance of their homes or difficulties with transportation. Despite the interest in participating, they did not manage to do so due to the need to be at the ambulatory on a weekly basis. Those who chose to participate in the therapy sessions were considered as the intervention group (IG)—aged between 42 and 69 years—and those who preferred not to participate in this phase of the experiment were considered as the control group (CG)—aged between 30 and 75 years. All participants in the two groups responded to the evaluation instruments before the treatment started.

The details of all steps of the treatment were clarified. Acromegalics attended weekly, one and a half hour group sessions that applied the technique “Think healthy and feel the difference” (23, 2730); for a total of 9 weeks. The IG was treated in the 3 month period from September to November 2015.

In the post-intervention step, after the end of the nine sessions of application of the technique, all IG and CG participants were submitted to evaluations with the aim of analyzing the effect of CBT on the IG. The results were compared between groups.

For the follow-up phase, in August 2016, 9 months after the end of the IG sessions, the IG and CG participants were once again submitted to evaluations. Three participants in the control group did not respond to the evaluation instruments. As a result, the total number of participants dropped from 23 to 20 (Figure 1).

Figure 1.

Figure 1

Sample composition and evaluation steps.

Evaluation Instruments

For acromegaly, AcroQol is the instrument used in 80% of studies to evaluate quality of life. It consists of 22 questions, 11 of them more directly related to physical alterations. Regarding the level of cognition, seven of the questions are conditional beliefs with emotional dysregulation of moderate intensity, as for example, item 8: “I feel rejected by people because of my illness.” Four of them are core beliefs with greater emotional dysregulation, for example, item 4: “I look awful in photographs.” Because of the risk of intense imbalance emotion, AcroQol questions were used only in the seventh session for the participants to identify their cognitive distortions, restructure them and build healthier behaviors.

Because of this, two self-administered evaluation instruments were answered by the participants of the two groups in the three stages of the present study: pre-intervention, post-intervention, and follow-up.

Quality of Life Questionnaire (SF-36)

The Short Form 36 Question Health Survey (SF-36) was used to evaluate quality of life (31). This is a multidimensional questionnaire, composed of 36 items, subdivided into eight sections with their respective questions: physical functional (item 03); role-physical (item 04); bodily pain (items 07 and 08); general health (items 01 and 11); vitality (options a, e, g, and i of item 09); social functioning (items 06 and 10); role-emotional (item 05), and mental health (options b, c, d, f, and h of item 09). In addition to the eight sections, item 02 is not part of the calculation of any section, being used only to evaluate how much the individual is better or worse compared to a year ago. It presents a final score of 0 (zero) to 100 (hundred), in which zero shows the worst state and 100 the best state (31).

Beck Depression Inventory (BDI)

The Beck Depression Inventory (BDI) was used to evaluate signs of depression (24). The following levels were considered for this scale, as they are for psychiatric patients: minimal: 0 to 11; mild: 12 to 19; moderate: 20 to 35; serious: 36 to 63. A score of 18 to 19 indicates likelihood of depression (24).

Intervention Protocol

The “Think healthy and feel the difference” protocol (23, 2730), adapted for patients with acromegaly, was applied in a group setting and all participants received printed material. The technique is available to download as an application for mobile devices at the Apple Store and Google Play, under the name “Think Healthy,” with versions in Portuguese and English. Patients allowed the researcher to record the sessions for later transcription.

A small, plastic, coping card, measuring 10 × 6 cm, with an illustration of the avocados, was delivered to encourage the practice of the techniques and healthy decision making in moments of emotional imbalance.

In each session, specific topics were covered. The content of the sessions was presented as follows: (1) basic concepts of CBT and practical examples of the relationship between unhealthy and healthy levels of cognition with emotion and associated behaviors; (2) emotional regulation; (3) increase self-esteem and self-confidence, and supply of a brain-shaped piggy bank (identification and valuation of personal qualities and achievements); (4) “Think healthy and feel the difference” technique—guidelines for completing the six steps adapted for the practice of physical activity; (5) the technique for approaching anger, assertiveness training, and the coping card; (6) the technique for approaching fear; (7) the technique adapted for shame about one's physical appearance in acromegaly; (8) clarifications on acromegaly, and (9) a summary of the topics covered in the sessions.

To consolidate knowledge and to assist in the practice of cognitive and behavioral skills between the therapy sessions, a therapy notepad and block of coping cards were provided (29).

Data Analysis

To verify the equivalence of profiles of both the control and the intervention groups, we performed the non-parametric Mann-Whitney U test for the scalar variables (32). For the categorical variables, Chi-square or Fisher's tests were performed (32).

To control the impact of non-randomization on the distribution in the groups, we performed covariance analysis (ANCOVA) to compare the SF-36 and BDI measurements in the post intervention period. The baseline means were used as covariates; thus, the groups were equalized by their baseline in the post-intervention comparison (33, 34).

In order to verify whether the clinical effect was sustained 9 months after the intervention, the same procedure to compare the measures post-intervention was done; however, to it was added the measures of the post-intervention as a covariant, as well as the baseline. Moreover, the comparison between the intervention and the control groups was made. Student's t-Test, paired, was used when comparing the measures of the baseline and of the post-intervention, and whether the clinical effect was sustained.

To interpret the size of the effects, Cohen's criterion was adopted: small (d′ < 0.3), moderate (0.3 ≤ d′ < 0.5), or large (d′ ≥ 0.5) (35). In all analyses, statistical significance was considered to be p < 0.05. In order to determine if the sample size was adequate for the effect size, thus avoiding a type II error, post-hoc analysis was made using the G*POWER 3.1 software, where the acceptable statistical power found was β = 0.80 (36, 37).

Results

Sixty-two acromegalics were selected from the endocrinology clinic of the University Hospital of Brasília. Thirty-nine of them did not agree to participate in the study, mainly because they could not attend the study site on a weekly basis. Thus, the sample consisted of 23 patients. There were 15 women (65.2%). Ages ranged from 30 to 75 years (mean = 52.78 ± 12.86 years, CV = 0.24, n = 23), from 42 to 69 years in the intervention group, and from 30 to 75 years in the control group. The mean time since disease diagnosis was 11.60 ± 7.14 years (CV = 0.62, n = 23). The time lag between the diagnosis and the beginning of the treatment ranged from 0.17 to 18 years (mean = 6.37 ± 4.94 years, CV = 0.78, n = 23). Regarding the stages of the disease, four (17.40%) were classified as cured, in 10 it was under control (43.50%), and in nine it was active (39.10%). The MRI assessment of the tumor showed the mean of the largest diameter was 23.36 ± 16.49 mm (CV = 0.71; n = 22). The percentage of IGF-1 levels (ULNR IGF-1) ranged from 30.30 to 384.30 (mean = 144.33 ± 85.00, CV = 0.59, n = 23). As for the treatment strategies, 20 (87%) underwent surgery, 21 (91.3%) used medication, and seven (30.40%) underwent radiotherapy. Regarding the level of depression, 11 (47.8%) presented minimal scores according to the BDI, six (26.1%) had mild scores, and six (26.1%) had moderate scores.

As shown on Table 1, there was no significant difference between all the variables studied: age, time since diagnosis, delay in diagnosis, largest tumor diameter in MRI, IGF-1 ULNR %, gender, disease activity, underwent therapies, and symptoms of depression. Among the variables in the study, only bodily pain presented significant differences (p = 0.002), where the control group had a higher score (mean = 66.67 ± 24.00) compared to the intervention one (mean = 38.89 ± 12.00).

Table 1.

Comparison between the control group and the intervention group in relation to age, gender, the clinical and laboratory aspects of the disease, and the study variables in the baseline (n = 23).

Control (n = 13) Intervention (n = 10) p-value*
Median (Q1–Q3) Median (Q1–Q3)
Age (years) 55.00 (50.0–62.0) 46.00 (37.8–58.3) 0.335
Time since diagnosis (years) 11.00 (4.8–19.3) 12.00 (8.75–16.5) 0.926
Delay in diagnosis (months) 48.00 (24.0–108.0) 84.00 (66.0–120.0) 0.532
Largest diameter in MRI (mm) 20.00 (17.0–27.0) 12.00 (11.3–49.5) 0.815
ULNR IGF-1 (%) 117.45 (109.8- 121.3) 118.70 (103.38–245.88) 0.664
f(%) f(%) p-value
Gender
Male 6 (46.15) 1 (10.00) 0.074
Female 7 (53.85) 9 (90.10)
Disease activity
Active 6 (46.15) 3 (30.00) 0.734
Controlled 5 (38.46) 5 (5.00)
Cured 2 (15.38) 2 (2.00)
Underwent surgery
Yes 12 (92.31) 8 (80.00) 0.560
No 1 (7.69) 2 (20.00)
Using acromegaly medication
Yes 11 (84.62) 10 (100.00) 0.486
No 2 (15.38) 0 (0.0)
Underwent radiotherapy
Yes 3 (23.08) 4 (40.00) 0.650
No 10 (76.92) 6 (60.00)
Symptoms of depression (BDI)
Minimal 7 (53.85) 4 (40.00) 0.805
Mild 3 (23.08) 3 (30.00)
Moderate 3 (23.08) 3 (30.00)
Study variables Mean Standard deviation Mean Standard deviation p-value
Physical functional 70.00 26.06 58.50 26.67 0.311
Role-physical 50.00 36.80 32.50 39.18 0.284
Bodily pain 66.67 24.00 38.89 12.00 0.002
General health 53.08 15.07 46.00 21.58 0.364
Vitality 58.85 14.74 55.00 10.00 0.487
Social functioning 62.50 27.95 67.50 14.67 0.614
Role-emotional 56.41 45.92 43.33 49.81 0.521
Mental health 67.08 20.73 62.00 15.23 0.523
Beck depression inventory 12.23 9.57 13.30 9.03 0.788

Q1, 1° Quartile; Q3, 3° Quartile;

*

Non-parametric Mann-Whitney test;

Chi-squared test;

t-test for repeated measurements.

The results of the effect of the treatment on the intervention group compared to the control one (patients who did not receive treatment) are presented in Table 2. Concerning the SF-36 sections, Vitality was higher in the control group (mean = 66.15 ± 9.61; p = 0.041; β > 0.80). However, Mental Health (mean = 76.80 ± 11.12) was higher in the intervention group when compared to the control group (mean = 68.92 ± 15.68; p = 0.025; β > 0.80). There were no significant differences between both groups in all the other sections. Regarding the BDI, no significant differences were observed between the groups either.

Table 2.

Effect of the treatment on the intervention group compared to the control group (no treatment) in relation to the quality of life questionnaire SF-36 and the Beck Depression Inventory (n = 23).

Control–post (n = 13) Intervention–post (n = 10) p-value§
Mean Standard deviation d post × pre Mean Standard deviation d' post × pre
Physical functional 66.92 26.34 −0.117 52.50 27.21 −0.223 0.481
Role-physical 59.62 47.37 0.228 65.00 42.82 0.793 0.252
Bodily pain 65.81 25.44 −0.035 50.00 17.57 0.752 0.705
General health 57.69 18.44 0.275 51.50 20.15 0.264 0.984
Vitality 66.15 9.61 0.600 54.50 14.03 −0.042 0.041
Social functioning 77.88 17.04 0.684 76.25 18.11 0.534 0.571
Role-emotional 53.85 48.19 −0.155 76.67 35.31 −0.243 0.740
Mental health 68.92 15.68 0.101 76.80 11.12 1.123* 0.025
Beck depression inventory 7.54 7.69 −0.544 12.50 8.49 −0.091 0.139

d′- d′ of Cohen;

*

t-test for repeated measurements p<0.01;

t-test for repeated measurements p < 0.05;

§

ANCOVA; Post: Intervention x Control, Covariant: Baseline (SF36 and BDI).

When comparing the baseline to the post-intervention, there was a significant increase in the score of General Health both in the control group (D′ = 0.280; P = 0.038; B > 0.80) and in the intervention one (D′ = 0.26; P = 0.024). Regarding the Vitality section, there was a significant increase only in the control group (D′ = 0.60; P = 0.022; β > 0.80). The score for Mental Health has a significant increase (P = 0.008), the greatest effect found (D′ = 1.123; β > 0.80). There were no significant differences in the other sections nor in the BDI evaluation.

Table 3 presents the adjustments measures for the ANCOVA models of the effect of the treatment in the intervention group compared to the control group, which did not receive the treatment, in the post-intervention. Concerning the SF-36, the sections were well-adjusted to the model, except for the Vitality variable (R2 = 0.176).

Table 3.

Adjustment measures for the ANCOVA models (n = 23) when comparing the control group (no treatment) to the intervention group in the post-intervention in relation to the quality of life questionnaire SF-36 and the Beck Depression Inventory.

Control (n = 13) Intervention (n = 10) R2 Base level standardization
Physical functional 62.88 57.75 0.647 65.00
Role-physical 53.89 72.44 0.334* 42.39
Bodily pain 57.37 60.98 0.339* 54.59
General health 55.00 54.94 0.639* 50.00
Vitality 65.81 54.95 0.176 57.17
Social functioning 78.77 75.10 0.225* 64.67
Role-emotional 50.99 80.38 0.292* 50.72
Mental health 67.77 78.29 0.477* 64.87
Beck depression inventory 7.76 12.21 0.311* 12.70

R2, Model adjustment;

*

p < 0.001.

Nine months after the end of the intervention, patients of both groups were again evaluated using SF-36 and BDI. Only the Mental Health section sustained a significant difference (p = 0.033) when comparing the control group (mean = 65.60 ± 15.91) to the intervention group (mean = 74.80 ± 21.25), in which case the intervention one had higher score (β > 0.80). The patients during the 9 months before the final evaluation had no changes in their disease stage.

The comparison between the post-intervention and the 9 month follow-up is presented in Table 4. The t-test for repeated measurements did not show significant difference either in the control group or the intervention group in any of the SF-36 sections or BDI.

Table 4.

Comparisons of follow up between the control and intervention groups in relation to the quality of life questionnaire SF-36 and the Beck Depression Inventory (n = 20).

Control–follow-up (n = 10) Intervention–follow-up (n = 10) p-value*
Mean Standard deviation d′ Mean Standard deviation d′
follow-up x post follow-up x post
Physical functional 69.50 24.43 0.041 50.00 27.59 −0.091 0.364
Role-physical 58.33 43.30 0.130 50.00 45.64 0.413 0.989
Bodily pain 56.67 20.59 −0.448 51.11 24.68 0.053 0.852
General health 54.00 16.47 −0.215 47.00 20.58 −0.221 0.255
Vitality 59.50 12.12 −0.562 50.00 14.14 −0.319 0.395
Social functioning 73.75 18.11 −0.296 65.00 27.51 −0.493 0.308
Role–emotional 55.56 47.14 −0.155 53.33 50.18 −0.546 0.970
Mental health 65.60 15.91 −0.133 74.80 21.25 −0.124 0.033
Beck depression inventory 11.40 12.02 0.424 10.60 6.24 −0.258 0.465

d′- d′ of Cohen;

*

ANCOVA, Post: Intervention x Control, Covariant: Baseline and Post (SF36 and BDI)

Table 5 presents the adjustment measures for the ANCOVA models when comparing the follow-up between the groups. Regarding the SF-36 instrument, only the Bodily Pain section (R2 = 0.156), General Health Perception (R2 = 0.141) and Mental Health (R2 = 0.351) were well-adjusted to the model.

Table 5.

Adjustment measures for the ANCOVA models (n = 20) when comparing the control group (no treatment) and the intervention one, during the follow-up, in relation to the quality of life questionnaire SF-36 and the Beck Depression Inventory.

Control (n = 10) Intervention (n = 10) R2 Base level standardization
Baseline Post
Physical Functional 64.215 55.285 0.488 63.75 60.50
Role-Physical 53.792 54.087 0.018 42.11 65.79
Bodily Pain 55.152 52.626 0.156* 52.22 58.33
General Health 55.645 45.355 0.141* 51.00 54.75
Vitality 57.384 52.116 0.221 57.25 60.25
Social Functioning 75.03 63.72 0.017 63.75 77.50
Role-Emotional 53.908 54.816 0.059 52.63 70.13
Mental Health 60.997 79.403 0.351* 63.60 72.20
Beck Depression Inventory 12.53 9.47 0.149 12.50 9.80

R2, Model adjustment;

*

p <0.01.

Discussion

The results showed that the application of the “Think Healthy” technique, for 9 weeks, resulted in an improvement in the quality of life in the intervention group when compared to the control group. This confirms the previous observation that the technique is useful in psychological support of acromegalics. (23). Furthermore, the present study supplements that the effect was maintained at a 9 month follow-up, which suggests stability in the effects produced by the treatment.

The strategy used here—nine sessions of group therapy—should be effective, since in groups with obsessive-compulsive disorder, a program of seven sessions was as effective as the same program conducted over 12 sessions (38).

Thus, the good long-term results, described here, of the use of CBT in improving quality of life in acromegalics fills a gap in the management of these patients. This is because, the psychotherapeutic approach has been described as important in other chronic diseases, but not in acromegaly (4).

Regarding the results achieved in the SF-36, in the intervention group, the mental health dimension had a significant increase, showing the greatest effect with the treatment (Table 4). In both groups there was an improvement in general health, which could be explained by the fact that all participants of the study where treated on the same neuroendocrinology outpatient clinic of the University Hospital of Brasília.

In the control group, the difference in the vitality variable should be interpreted with caution, since it did not present a good fit for the model (R2 = 0.176) (Table 3). This result shows the need of having other studies as well to try and explain this finding. What could have happened is that the IG participants have learned to observe themselves while the CG participants stayed lenient to their evaluation. The other dimensions did not show significant differences, although some presented moderate and large effects, and fitted the model well.

The improvement in quality of life after treatment and the fact that it was maintained after a 9 month follow-up may have been facilitated by the characteristics of CBT. The intervention stimulates visual memory, because it uses visual, verbal, and written support. Tasks based on CBT require planning and execution—executive function—and can be considered cognitive training. Socratic questioning—characteristic of the systematization of the technique in its six stages—favors the learning and active participation of patients in their treatment process (18).

In terms of outcome and maintenance of the achieved improvement, the results of this research are similar to those obtained in other studies on other diseases. Improvements achieved in obsessive-compulsive symptoms were maintained in evaluations after a 1-year (38) and a 2-year follow-up (39). Positive results were also achieved and maintained in follow-ups for other disorders: anxiety in young people (40), obesity with binge eating (41), general anxiety, (42) psychiatric disorders in comorbidity (43), compulsive shopping (44), social anxiety (17), and body dysmorphic disorder in adolescents (45).

The results described here, using CBT to improve quality of life, are of particular importance because it is still uncertain whether the control of the disease is associated with some gain in this parameter. For example, with biochemical control of acromegaly, a study with a longer duration of follow-up (mean follow-up 5.7 ± 0.6 years) did not show improvement in quality of life when compared to the control group (46). These authors emphasized that addressing physical and psycho-social comorbidities is as important as the biochemical control of the disease (46). This study (45) evaluated the quality of life of 106 surgically treated patients, 3 and 12 months after the surgical intervention. Regarding the SF-36, there was improvement in all dimensions, but it was not statistically significant (47).

On the other hand, a study that used the SF-36 to evaluate the quality of life of 41 acromegalics before surgery, after surgery, and at a 1-year follow-up, showed a statistically significant improvement in the following dimensions: role-physical, general health, social functioning, and mental health (7). These results were similar to those described in this study for the domains of general health and mental health.

The short-lasting treatment and the possibility of recurrence at the end of the treatment are of real concern; however, in the present study the results were maintained at a 9-month follow-up. Some participants reported the benefits of the group format for learning coping strategies. This may be because learning and living experiences, such as psychotherapy, can induce epigenetic changes in brain circuits, similar to the effect of medication (48). When pharmacology is combined with psychotherapy, due to therapeutic synergy, the result tends to be greater than the sum of the two treatments (1 + 1 = 3) (48).

In the present study, the BDI score levels of the psychiatric patients (i.e., minimum, mild, moderate, and severe) were used because of the lack of a cutoff point for patients with acromegaly. In the pre-intervention assessment, three participants showed an indication of moderate depression, three showed mild depression, and four showed minimal depression. No participant in the present study showed an indication of severe depression. The lowest depression score possible (i.e., zero) was found in only one study participant. In that case, no improvement was possible, which is considered a floor effect. In addition, the decrease in BDI score was not significant.

Even though there is no gender difference between both groups, there was a tendency, which may point to a limitation in the generalization of the study. For this reason, the authors suggest that new gender stratification studies be carried in the future.

A limitation of the present study is the small case-by-case analysis; however, acromegaly is a rare disease. In addition, we used a convenience sample, in which the patients presented for the treatment, rather than a random sample. However, the psychotherapeutic approach was showed to reduce the suffering and improve the quality of life for acromegalics, with good short- and long-term results. The results achieved by this study reinforce the importance of more research on the use of cognitive-behavioral techniques in different clinical contexts.

Ethics Statement

The research project was approved by the Research Ethics Committee (CEP) of the Faculty of Health Sciences of the University of Brasília—UnB. A Free and Informed Consent form was read and signed by the participants of the group.

Author Contributions

LK, LC, and LN analyzed the patient data. LK and LC were major contributions in writing the manuscript. LK is a cognitive-behavioral therapist by The Beck Institute and conducted the cognitive-behavioral group sessions. All authors agreed to be accountable for the content of the work and approved the submitted version of the manuscript.

Conflict of Interest Statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Glossary

Abbreviations

BDI

beck depression inventory

CBT

cognitive-behavioral therapy

CG

control group

GH

growth hormone

IG

intervention group

IGF

insulin-like growth factor-1

MRI

magnetic resonance imaging

SF-36

quality of life questionnaire.

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